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THE GOVERNMENT
OF VIETNAM
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SOCIALIST REPUBLIC OF VIETNAM
Independence - Freedom - Happiness
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No. 21/2026/NQ-CP
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Hanoi, April 29, 2026
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RESOLUTION
ON REDUCTION AND SIMPLIFICATION OF
BUSINESS CONDITIONS, ADMINISTRATIVE PROCEDURES AND DELEGATION OF AUTHORITY TO
ADMINISTER ADMINISTRATIVE PROCEDURES IN THE HEALTH SECTOR
Pursuant to the Law on
Organization of the Government No. 63/2025/QH15;
Pursuant to the Law on
Organization of Local Government No. 72/2025/QH15;
Pursuant to the Law on
Promulgation of Legislative Documents No. 64/2025/QH15, amended in 2025 by Law
No. 87/2025/QH15;
At the proposal of the Minister of Health;
The Government hereby
issues a Resolution on the reduction and simplification of business conditions,
administrative procedures and delegation of authority to administer
administrative procedures in the health sector.
Article
1. Scope
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Article
2. Delegation of authority to administer administrative procedures in the
health sector
1. Delegation of authority to administer administrative
procedures on food safety:
a) The issuance of
certificates of advertising content approval for health supplements as
prescribed in clause 5 Article 27 of Decree No. 15/2018/ND-CP elaborating on certain
articles of the Law on Food Safety shall fall under the authority of the
President of the province-level People's Committee;
b) The application and
procedures shall be carried out in accordance with Appendix I issued together
with this Resolution.
2. Delegation of authority to administer administrative
procedures on disease prevention:
a) The application for
import of biological specimens as prescribed in Article 36 of Decree No.
89/2018/ND-CP elaborating on certain articles of the Law on Prevention and
Control of Infectious Diseases on border health quarantine, amended by Decree
No. 155/2018/ND-CP, shall fall under the authority of the President of the
province-level People's Committee;
b) The application and
procedures shall be carried out in accordance with Appendix II issued together
with this Resolution.
3. Delegation of authority to administer administrative
procedures on issuance of licenses to practice medicine:
a) The issuance,
re-issuance, renewal, adjustment, suspension, or revocation of the license to
practice medicine (including practicing certificates issued under the Law on
Medical Examination and Treatment No. 40/2009/QH12, hereinafter referred to as
the license to practice medicine, for regulated entities prescribed in point a
clause 1 Article 28 of the Law on Medical Examination and Treatment and clause
8 Article 143 of Decree No. 96/2023/ND-CP elaborating on certain articles of
the Law on Medical Examination and Treatment) as prescribed in clause 6 Article
14, clause 15 Article 16, clause 2 Article 18, clause 3 Article 20, clause 7
Article 22, clause 9 Article 24, clause 2 Article 26, clause 5 Article 130,
clause 18 Article 132, clause 2 Article 134, clause 4 Article 136 of Decree No.
96/2023/ND-CP shall fall under the authority of the President of the
province-level People's Committee;
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4. Delegation of authority to administer administrative
procedures on issuance of health facility operating licenses:
a) The authority to
re-issue and adjust the health facility operating license in cases of change of
working hours or change of name or address of the healthcare facility without
change of location for private hospitals, as prescribed in Article 63 and
Article 65 of Decree No. 96/2023/ND-CP, shall fall under the authority of the
President of the province-level People's Committee;
b) The application and
procedures shall be carried out in accordance with Appendix IV issued together
with this Resolution.
Article
3. Reduction and simplification of business conditions in the health sector
1. Business conditions relating to biosafety at laboratories as
prescribed in Articles 5, 6 and 7 of Decree No. 103/2016/ND-CP on ensuring
biosafety at laboratories, amended by Decree No. 155/2018/ND-CP, shall no
longer apply.
2. Business conditions relating to vaccination services as
prescribed in Article 9 and Article 10 of Decree No. 104/2016/ND-CP on
vaccination activities, amended by Decree No. 155/2018/ND-CP, shall no longer
apply.
3. Business conditions relating to the organization of clinical
training in health science education as prescribed in Article 8, Article 9,
clause 2 Article 10 and Article 11 of Decree No. 111/2017/ND-CP on the
organization of clinical training in health science education and Article 140
of Decree No. 96/2023/ND-CP, shall no longer apply.
4. Business conditions relating to the provision of opioid
substitution therapy (OST) services as prescribed in Article 16 and Article 17
of Decree No. 141/2024/ND-CP elaborating on certain articles of the Law on
Prevention and Control of HIV/AIDS, shall no longer apply.
5. Business conditions relating to the provision of HIV
counseling and testing services as prescribed in clause 2 Article 38, Article
39, Article 40 and Article 41 of Decree No. 141/2024/ND-CP and clauses 1 and 2
Article 5 of Decree No. 63/2021/ND-CP elaborating on the Law on amendments to
the Law on Prevention and Control of HIV/AIDS, shall no longer apply.
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Article
4. Reduction and simplification of administrative procedures in the health
sector
1. The following administrative procedures shall no longer be
required:
a) The procedure for
registration of product declaration for compound food additives with new uses,
food additives not listed in the list of additives permitted for use in food,
or food additives used for unintended purposes as prescribed by the Ministry of
Health under clause 3 Article 6 of Decree No. 15/2018/ND-CP;
b) The procedures for new
issuance, re-issuance, self-certification and revocation of certificates of
biosafety-compliant laboratories as prescribed in Articles 11, 12, 13 and 14 of
Decree No. 103/2016/ND-CP, amended by Decree No. 155/2018/ND-CP;
c) The procedure for
declaration of eligibility to provide vaccination services as prescribed in
Article 11 of Decree No. 104/2016/ND-CP, amended by Decree No. 155/2018/ND-CP;
d) The procedure for
declaration of eligibility to provide opioid substitution therapy (OST)
services as prescribed in Articles 19, 20, 21 and 22 of Decree No.
141/2024/ND-CP;
dd) The procedures for new
issuance, re-issuance, adjustment and revocation of certificates of eligibility
for confirmatory HIV testing, or decisions on designation, adjustment
decisions, revocation of designation decisions for reference confirmatory HIV
testing laboratories, and suspension of confirmatory HIV testing or reference
confirmatory HIV testing operations as prescribed in Articles 42, 43, 44 and
45; point b clause 1, point b clause 7, clause 8 Article 46 and Article 47 of
Decree No. 141/2024/ND-CP;
e) The procedure for
issuance of certificates to educational establishments meeting the conditions
for examination and recognition of proficiency in Vietnamese or other languages
or qualification as interpreter in medical examination and treatment as
prescribed in Article 141 and Article 142 of Decree No. 96/2023/ND-CP.
2. Simplification of administrative procedures in the field of
medical examination and treatment:
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"3. Within 10 working
days from the date recorded on the acknowledgement of receipt of the
declaration as prescribed in clause 3 Article 6 of Decree No. 96/2023/ND-CP,
the receiving authority shall be responsible for publishing information of the
clinical training facility on its online portal or website and on the health
facility management information system.
Where the requirements are
not met, the receiving authority shall send a written notice to the healthcare
facility stating the reasons.
The minimum information to
be published shall include: name and address of the clinical training facility, scope of
clinical training guidance (where there are affiliated facilities involved in
practical training guidance, the content and name of the affiliated clinical
training facility must also be published), and cost of clinical training
guidance.
Where the receiving
authority fails to send a written notice to the healthcare facility regarding
the ineligibility as a clinical training facility or fails to publish
information as prescribed in clause 4 Article 6 of Decree No. 96/2023/ND-CP
within 10 working days from the date recorded on the acknowledgement of receipt
of the declaration, the clinical training facility may commence its clinical
training guidance operations";
b) Reduction of processing
time for the procedure for application for recognition of a license to practice
medicine issued by a competent foreign authority or organization as prescribed
in points b and c clause 3 Article 37 of Decree No. 96/2023/ND-CP, as follows:
"b) Where the
applicant for recognition of the license to practice medicine holds a license
issued by a foreign licensing authority or organization that has already been
assessed for recognition:
- Within 20 working days from the date of receipt of the
application, the Ministry of Health shall issue a written response on whether
or not the license to practice medicine is recognized;
- Where verification of the practitioner's overseas training
is required, the recognition period shall be 20 working days from the date of
receipt of the verification results.
c) Where the applicant for
recognition of the license to practice medicine holds a license issued by a
foreign licensing authority or organization that has not yet been assessed for
recognition:
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- Within 20 working days from the date of the assessment
results for recognition, the Ministry of Health shall issue a written response
on whether or not the license to practice medicine is recognized;
- Where verification of the practitioner's overseas training
is required, the recognition period shall be 20 working days from the date of
receipt of the verification results.";
c) Reduction of processing
time for the procedure for new issuance of a health facility operating license
as prescribed in Article 61 of Decree No. 96/2023/ND-CP, as follows:
"1. Submit 1 set of
documents for new issuance and pay fees and charges as prescribed by law on
fees and charges to the competent authority for issuance of the operating
license (hereinafter referred to as the licensing authority).
2. Upon receipt of the application, the receiving authority
shall issue to the applicant an acknowledgement of receipt in accordance with
Form 02 Appendix I issued together with this Decree.
3. Where no amendment to the application is required:
a) The licensing authority
shall conduct an assessment of operating conditions and the list of approved
medical procedures at the applicant's facility and prepare an assessment report
within 40 days from the date recorded on the acknowledgement of receipt;
b) Where no amendment is
required, the licensing authority shall issue the new operating license and
issue a decision approving the list of approved medical procedures at the
facility within 10 working days from the date of the assessment report;
c) Where amendments are
required, these shall be clearly stated in the assessment report.
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4. Where amendment to the application is required:
a) The licensing authority
shall send a written notice to the applicant specifying the documents and
particulars requiring amendment within 10 working days from the date recorded
on the acknowledgement of receipt.
b) Upon amending the
application, the applicant shall send a written notice and supporting documents
proving completion of the amendments.
c) Upon receipt of the
amended application, the licensing authority shall be responsible for following
the procedures as prescribed:
- Under clause 3 of this Article where no further amendments
are required;
- Under points a and b of this clause where the applicant has
made amendments but the requirements are not yet met.
5. Within 5 working days from the date of issuance of the
operating license, the licensing authority shall publish on its online portal
and on the health facility management information system the following
information: name
and address of the licensed facility; full name and license number of the person
responsible for professional and technical matters; operating license number;
scope of professional practice and professional operating hours.
6. The operating license shall be prepared in 2 copies in
accordance with Form No. 06 Appendix II issued together with this Decree: 1 copy for the applicant
and 1 copy retained by the licensing authority, except where results have been
returned through electronic means.
7. Where the facility is granted an operating license in the
form of a hospital, upon issuance of the operating license, the licensing
authority shall issue a document provisionally classifying the hospital at the
basic level. The
provisional classification period shall be 2 years from the date recorded on
the provisional classification document. Within 60 days before the end of the provisional
classification period, the hospital shall submit an application for the
procedure for professional and technical classification in accordance with
Article 90 of this Decree.";
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"1. Submit 1 set of
documents as prescribed in clause 2 Article 64 of this Decree and pay fees and
charges as prescribed by law on fees and charges to the licensing authority.
2. Upon receipt of the application, the licensing authority
shall issue to the applicant an acknowledgement of receipt.
3. Where amendment to the application is required, within 7
working days from the date recorded on the acknowledgement of receipt, the licensing
authority shall send a written notice to the applicant specifying the documents
and particulars requiring amendment.
Within 6 months from the
date of the licensing authority's written notice requesting amendments, the
applicant shall submit the amended application as required. After this period, where
the applicant fails to make amendments, the submitted application shall become
invalid.
4. Upon receipt of the amended application, the licensing
authority shall issue to the applicant an acknowledgement of receipt for the
amended application:
Where the amended
application does not meet the requirements, the licensing authority shall send
a written notice to the applicant as prescribed in clause 3 of this Article.
Within 6 months from the
date of the licensing authority's written notice requesting amendments, the
applicant shall submit the amended application as required.
After this period, where
the applicant fails to make amendments, or after 12 months from the date of the
initial submission where the amended application still does not meet the
requirements, the submitted application shall become invalid.
5. Where no amendment to the application is required, or where
the application has been completed as prescribed in clauses 3 and 4 of this
Article, the licensing authority shall:
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b) Conduct an on-site
assessment at the applicant's facility and prepare an assessment report within
40 days from the date recorded on the acknowledgement of receipt where on-site
assessment is required; the assessment report shall clearly state any
requirements for amendment (if any).
6. Following on-site assessment, the licensing authority shall
be responsible for:
a) Issuing a document
permitting the change of operational scale, scope of professional practice, or
addition or reduction of the list of approved medical procedures within 10
working days from the date of the assessment report where no amendments are
required;
b) Issuing a written
notice of matters requiring remediation and rectification within 5 working days
from the date of the assessment report where amendments are required.
Within 6 months from the
date of the licensing authority's written notice regarding matters requiring
amendment, where the applicant fails to complete the amendments, the submitted
application shall become invalid.
7. Within 10 working days from the date of receipt of the
written notice and supporting documents proving completion of amendments by the
applicant, the licensing authority shall:
a) Issue a document permitting
the change of operational scale, scope of professional practice, or addition or
reduction of the list of approved medical procedures where no on-site
inspection of the amendments is required.
b) Conduct an on-site
inspection of the amendments where required:
- Issue a document permitting the change of operational scale,
scope of professional practice, or addition or reduction of the list of
approved medical procedures where the applicant has completed the amendments;
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8. Within 5 working days from the date of permission for
addition to the list of approved medical procedures, the licensing authority
shall publish and update on its online portal or website and on the health
facility management information system all information relating to the adjusted
content.
9. The document permitting addition to the list of approved
medical procedures shall be prepared in 2 copies:
1 copy for the applicant and 1 copy retained by
the licensing authority, except where results have been returned through
electronic means.
10. Where addition of special-category medical procedures to the
list of approved medical procedures is requested:
a) The healthcare facility
shall submit 1 set of documents as prescribed in clause 2 Article 64 of this
Decree to the Ministry of Health to request consideration of the facility's
capability to perform special-category medical procedures.
b) Within 5 working days
from the date of receipt of the application, the Ministry of Health shall
examine and evaluate the level and capability of the healthcare facility to
perform these special-category medical procedures to determine whether a pilot
is required or whether the healthcare facility has sufficient conditions to
conduct the pilot.
c) Where a pilot of
special-category medical procedures is required, the process shall be carried
out in accordance with Article 97 of this Decree.
d) Where the healthcare
facility has completed the pilot of special-category medical procedures and has
submitted a written report on the pilot results proposing official deployment
of the special-category medical procedures, the following steps shall be taken:
- The healthcare facility shall submit 1 set of documents
including the pilot results report for special-category medical procedures as
prescribed in point c of this clause and the technical procedure proposed by
the healthcare facility;
- Within 10 working days from the date of receipt of a
complete application, the Ministry of Health shall conduct an assessment of the
pilot results and the technical procedure proposed by the healthcare facility;
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- The healthcare facility shall follow the procedures
prescribed in clauses 1 through 9 of this Article to add the officially permitted
special-category medical procedures to its scope of professional practice.
dd) Where no pilot of
special-category medical procedures is required, the following procedures shall
be followed:
- Within 5 working days, the Ministry of Health shall issue a
decision permitting the healthcare facility to officially apply the
special-category medical procedures without conducting a pilot. Where approval is not
granted, a written response stating the reasons shall be provided;
- The healthcare facility shall follow the procedures
prescribed in clauses 1 through 9 of this Article to add the officially
permitted special-category medical procedures to its scope of professional
practice.".
Article
5. Implementation
1. The Ministry of Health shall be responsible for monitoring,
urging and inspecting the implementation of this Resolution.
2. Ministers, heads of ministerial agencies, and Presidents of
People's Committees of provinces and centrally-affiliated cities shall
implement this Resolution.
3. People's Councils, committees of People's Councils, deputies
of People's Councils, and the Vietnam Fatherland Front at all levels shall,
within the scope of their duties and powers, strengthen oversight of the
implementation of this Resolution.
4. Heads of agencies and units, cadres, civil servants and
public employees who participated in the drafting and issuance of this
Resolution shall be considered for exclusion, exemption or reduction of
liability in accordance with clause 11 Article 68 of the Law on Promulgation of
Legislative Documents No. 64/2025/QH15, amended by Law No. 87/2025/QH15.
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1. This Resolution comes into force from April 29, 2026 to
January 1, 2028, except as provided in clauses 2 and 3 of this Article.
2. The provisions of Article 2 of this Resolution shall come
into force from July 1, 2026.
3. The provisions of Article 3 and clause 1 Article 4 of this
Resolution shall come into force from July 1, 2027.
4. During the period this Resolution is in force, where any law
or resolution of the National Assembly, ordinance or resolution of the National
Assembly Standing Committee, or decree or resolution of the Government contains
provisions on administrative procedures relating to the provisions of this
Resolution that are adopted or issued, the corresponding provisions of this
Resolution shall cease to be in force at the time such legislative documents
come into force.
5. Applications for settlement of administrative procedures in
the fields prescribed in Articles 2, 3 and 4 of this Resolution and the
Appendices issued together herewith that have been received by a competent
authority or have been postmarked before this Resolution comes into force shall
be processed in accordance with the law in force governing that field at the
time the application was received.
6. During the period the provisions of this Resolution are in
force, where the provisions on administrative procedures and business
conditions in this Resolution differ from related legislative documents falling
under the jurisdiction of the Government or the Prime Minister, the provisions
of this Resolution shall apply.
ON
BEHALF OF GOVERNMENT
PP. PRIME
MINISTER
DEPUTY PRIME MINISTER
Pham Thi Thanh Tra
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APPENDIX I
APPLICATION AND PROCEDURES FOR
APPROVAL OF ADVERTISING CONTENT FOR HEALTH SUPPLEMENTS
(Issued together with Resolution No. 21/2026/NQ-CP dated April 29, 2026 of the
Government)
1. Organizations and individuals with products to be advertised
shall prepare 1 set of documents for registration of advertising content
approval and submit in person or through the online public service system of
the province-level People's Committee (hereinafter referred to as the receiving
authority);
The application shall
include:
a) Application form for
registration of advertising content approval in accordance with Form No. 10
Appendix 1 issued together with Decree No. 15/2018/ND-CP dated February 2, 2018
of the Government elaborating on certain articles of the Law on Food Safety;
b) Receipt of registration
of product declaration and the product declaration confirmed by a competent
authority, or the receipt of the product conformity declaration/certificate of
conformity with food safety regulations that is still valid (copy bearing
confirmation of the organization or individual);
c) Product label sample
(copy bearing confirmation of the organization or individual);
d) For advertising on
radio or television, a proposed advertising script and proposed advertising
content recorded on video disc or audio disc shall be required; for advertising
through other media, a mock-up (sample advertising content) of the proposed
advertising shall be required (copy bearing confirmation of the organization or
individual);
dd) For advertising
content beyond the uses and functions of the product stated in the product
declaration, scientific documentation as evidence shall be required (copy
bearing confirmation of the organization or individual);
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2. Within 10 working days from the date of receipt of a
complete and valid application, the receiving authority shall be responsible
for reviewing the application and returning results in accordance with Form No.
11 Appendix 1 issued together with Decree No. 15/2018/ND-CP. This period shall be
calculated from the date the complete application is received through the
online public service system.
Where the receiving
authority does not approve the advertising content of the organization or
individual, or requires amendment, the receiving authority shall issue a
written notice stating the reasons and legal basis for the request. Amendments may only be
requested once.
3. Within 10 working days from the date of receipt of the
amended application, the receiving authority shall assess the application and
issue a written response. After 90 working days from the date of the written notice
requesting amendments, where the organization or individual fails to make
amendments, the application shall become invalid.
4. The receiving authority shall be responsible for publicly
announcing the names and products of organizations and individuals that have
been issued certificates of advertising content approval for food products on
its website and the food safety database.
APPENDIX II
APPLICATION AND PROCEDURES FOR
ISSUANCE OF IMPORT PERMITS FOR BIOLOGICAL SPECIMENS CAPABLE OF CAUSING
INFECTIOUS DISEASES IN HUMANS
(Issued together with Resolution No. 21/2026/NQ-CP dated April 29, 2026 of the
Government)
1. The establishment applying for an import permit shall submit
1 set of documents in person, by post or online to the province-level People's
Committee in the local area (hereinafter referred to as the receiving
authority);
2. The application shall include:
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b) One of the following
documents proving the purpose of importation: certified copy of a valid decision by a competent authority
approving a research project or study still in force; certified copy of the
approved research proposal or project document; certified copy of a valid
agreement between the domestic establishment and the foreign establishment on
importation of biological specimens; other relevant supporting documents;
c) One of the following
documents proving that the laboratory belonging to the applicant, or the
laboratory hired or affiliated by the applicant to receive and store biological
specimens, meets biosafety requirements, including: self-certification of
compliance with biosafety standards for biosafety level I or level II testing
laboratories; certificate of biosafety compliance for biosafety level III testing
laboratories.
3. Procedures:
a) The establishment
applying for a permit shall submit the application as prescribed in clause 1 of
this Appendix;
b) Within 10 working days
from the date recorded on the acknowledgement of receipt, the receiving authority
shall review and issue the import permit for biological specimens in accordance
with Form No. 02 in Appendix II issued together herewith;
c) Where the application
is incomplete or invalid, within 10 working days from the date recorded on the
acknowledgement of receipt, the health professional authority under the
province-level People's Committee in the local area shall issue a written
notice requesting amendment of the application;
d) Within 30 days from the
date of receipt of the request for amendment, the establishment applying for a
permit shall complete the application as required.
Form No. 01
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SOCIALIST REPUBLIC OF VIETNAM
Independence - Freedom - Happiness
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No. /
Re: ………………
[1]......., [date]..................
APPLICATION FORM FOR IMPORT
PERMIT FOR BIOLOGICAL SPECIMENS
To: [LICENSING AUTHORITY]
The content of this
official letter shall include:
- Basis for importation of biological specimens
- Information on the biological specimens to be imported
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- Purpose of importation;
- Type of specimen;
- Origin;
- Quantity;
- Packaging method;
- Place of dispatch;
- Place of receipt;
- Route of transportation;
+ Commitment of the
importing (exporting) unit on biosafety, biosecurity and management of infectious
agents in accordance with applicable legal regulations on biological specimens.
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+ Full name and phone
number of the responsible officer.
Recipients:
- As above;
- Filed:
HEAD OF UNIT
(Signature and seal)
_____________________
[1] Location.
Form No. 02
PEOPLE'S COMMITTEE OF [PROVINCE]
[LICENSING AUTHORITY]
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No. /………
Re: import permit for biological specimens
[Location]......., [date]..................
To: [NAME OF IMPORTING UNIT]
In response to the
application form for an import permit for biological specimens of [NAME OF
IMPORTING UNIT] No.…… regarding the request for permission to import biological
specimens, [LICENSING AUTHORITY] provides the following response:
1. [NAME OF IMPORTING UNIT] is hereby approved to import
biological specimens with the following particulars: Purpose of importation;
Type of specimen; Origin; Quantity; Packaging method; Place of dispatch; Place
of receipt; Route of transportation; Other information as needed (which may be
listed in detail in an Appendix attached to this document).
2. [NAME OF IMPORTING UNIT] shall bear full responsibility for
compliance with regulations on biosafety, biosecurity and management of
infectious agents in accordance with applicable legal regulations.
[LICENSING AUTHORITY]
hereby notifies [NAME OF IMPORTING UNIT] for information and implementation.
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[HEAD OF LICENSING AUTHORITY]
(Signature, full name and seal)
APPENDIX III
APPLICATION AND PROCEDURES FOR NEW
ISSUANCE, RE-ISSUANCE, ADJUSTMENT, RENEWAL, SUSPENSION, AND REVOCATION OF THE
LICENSE TO PRACTICE MEDICINE UNDER THE LAW ON MEDICAL EXAMINATION AND TREATMENT
(Issued together with Resolution No. 21/2026/NQ-CP dated April 29, 2026 of the
Government)
Part 1. Application and
procedures for new issuance of the license to practice medicine
1. During the period from the effective date of this Resolution
to December 31, 2026, the procedures for new issuance of the license to
practice medicine for practitioners with the professional title of physician,
medical assistant, nurse, midwife, medical technician, clinical nutritionist,
emergency medical responder (EMR), or clinical psychologist shall be carried
out as follows:
a) The applicant for the
license to practice medicine shall submit 1 set of documents corresponding to
each case prescribed in clauses 1 through 4 Article 130 of Decree No. 96/2023/ND-CP
(in person, by post or through electronic means) and pay fees and charges as
prescribed by law on fees and charges to the province-level People's Committee
(hereinafter referred to as the receiving authority);
b) The receiving authority
shall issue the license to practice medicine within 20 working days from the
date of receipt of a complete application. Where the license to practice medicine is not issued, a
written response stating the reasons shall be provided.
Where verification of
documents with foreign elements in the application for the license to practice
medicine is required, the period for issuance of the license to practice
medicine shall be 20 working days from the date of receipt of the verification
results.
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a) The applicant for the
license to practice medicine shall submit 1 set of documents corresponding to
each case prescribed in clauses 1 through 5 Article 14 of Decree No.
96/2023/ND-CP (in person, by post or through electronic means) and pay fees and
charges as prescribed by law on fees and charges to the receiving authority;
b) The receiving authority
shall issue the license to practice medicine within 20 working days from the date
of receipt of a complete application. Where the license to practice medicine is not issued, a
written response stating the reasons shall be provided.
Where verification of
documents with foreign elements in the application for the license to practice medicine
is required, the period for issuance of the license to practice medicine shall
be 20 working days from the date of receipt of the verification results.
3. The procedures for new issuance of the license to practice
medicine for practitioners with the professional title of traditional medicine
practitioner, holder of a hereditary medicinal formula or hereditary treatment
method shall be carried out as follows:
a) The applicant for the
license to practice medicine shall submit 1 set of documents corresponding to
each case prescribed in clauses 1 through 6 Article 22 of Decree No.
96/2023/ND-CP (in person, by post or through electronic means) and pay fees and
charges as prescribed by law on fees and charges to the receiving authority;
b) The receiving authority
shall issue the license to practice medicine within 30 days from the date of
receipt of a complete application. Where the license to practice medicine is not issued, a
written response stating the reasons shall be provided.
Where verification of documents
with foreign elements in the application for the license to practice medicine
is required, the period for issuance of the license to practice medicine shall
be 20 working days from the date of receipt of the verification results.
Part 2. Application and
procedures for re-issuance of the license to practice medicine
1. During the period from the effective date of this Resolution
to December 31, 2026, the procedures for re-issuance of the license to practice
medicine for practitioners with the professional title of physician, medical
assistant, nurse, midwife, medical technician, clinical nutritionist, emergency
medical responder (EMR), or clinical psychologist shall be carried out as
follows:
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b) The receiving authority
shall re-issue the license to practice medicine within 10 working days from the
date of receipt of a complete application; where the license to practice
medicine is not re-issued, a written response stating the reasons shall be
provided;
c) Where verification of
documents with foreign elements in the application for re-issuance of the
license to practice medicine is required, the re-issuance period shall be 10
working days from the date of receipt of the verification results.
2. From January 1, 2027, the procedures for re-issuance of the
license to practice medicine for practitioners with the professional title of
physician, medical assistant, nurse, midwife, medical technician, clinical
nutritionist, emergency medical responder (EMR), or clinical psychologist shall
be carried out as follows:
a) The applicant for
re-issuance of the license to practice medicine shall submit 1 set of documents
for re-issuance of the license to practice medicine corresponding to each case
prescribed in clauses 1 through 14 Article 16 of Decree No. 96/2023/ND-CP (in
person, by post or through electronic means) and pay fees and charges as
prescribed by law on fees and charges to the receiving authority;
b) The receiving authority
shall re-issue the license to practice medicine within 10 working days from the
date of receipt of a complete application; where the license to practice
medicine is not re-issued, a written response stating the reasons shall be
provided;
c) Where verification of
documents with foreign elements in the application for re-issuance of the
license to practice medicine is required, the re-issuance period shall be 10
working days from the date of receipt of the verification results.
3. The procedures for re-issuance of the license to practice
medicine for practitioners with the professional title of traditional medicine
practitioner, holder of a hereditary medicinal formula or hereditary treatment
method shall be carried out as follows:
a) The applicant for
re-issuance of the license to practice medicine shall submit 1 set of documents
for re-issuance of the license to practice medicine corresponding to each case
prescribed in clauses 1 through 8 Article 24 of Decree No. 96/2023/ND-CP (in
person, by post or through electronic means) and pay fees and charges as
prescribed by law on fees and charges to the receiving authority;
b) The receiving authority
shall re-issue the license to practice medicine within 10 working days from the
date of receipt of a complete application; where the license to practice
medicine is not re-issued, a written response stating the reasons shall be
provided;
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Part 3. Application and
procedures for renewal of the license to practice medicine
1. During the period from the effective date of this Resolution
to December 31, 2026, the procedures for renewal of the license to practice
medicine for practitioners with the professional title of physician, medical
assistant, nurse, midwife, medical technician, clinical nutritionist, or
emergency medical responder (EMR) shall be carried out as follows:
a) The applicant for
renewal of the license to practice medicine shall submit 1 set of documents as
prescribed in clause 1 Article 134 of Decree No. 96/2023/ND-CP (in person, by
post or through electronic means) and pay fees and charges as prescribed by law
on fees and charges to the receiving authority at least 40 working days before
the expiry date of the license to practice medicine;
Where the practitioner is
ill, injured or in a force majeure circumstance at the time of submission of
the renewal application, a written notice shall be sent to the receiving
authority to defer the submission of the renewal application for the license to
practice medicine;
The practitioner may
request deferral of the renewal date multiple times, but the total deferral
period shall not exceed 22 months from the expiry date of the license to
practice medicine;
b) During the period from
receipt of a complete application to the expiry date recorded on the license to
practice medicine, the receiving authority shall be responsible for carrying
out the renewal or providing a written response stating the reasons where the
renewal is not carried out; where no written response is provided by the expiry
date recorded on the license to practice medicine, the license to practice
medicine shall continue to be in force as prescribed;
c) Where verification of
the practitioner's continuing medical education (CME) under a program conducted
by a foreign authority or organization is required, the renewal period shall be
10 working days from the date of receipt of the verification results.
2. From January 1, 2027, the procedures for renewal of the license
to practice medicine for practitioners with the professional title of
physician, medical assistant, nurse, midwife, medical technician, clinical
nutritionist, or emergency medical responder (EMR) shall be carried out as
follows:
a) The applicant for
renewal of the license to practice medicine shall submit 1 set of documents as
prescribed in clause 1 Article 18 of Decree No. 96/2023/ND-CP (in person, by
post or through electronic means) and pay fees and charges as prescribed by law
on fees and charges to the receiving authority at least 40 working days before
the expiry date of the license to practice medicine;
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The practitioner may
request deferral of the renewal date multiple times, but the total deferral period
shall not exceed 22 months from the expiry date of the license to practice
medicine;
b) During the period from
receipt of a complete application to the expiry date recorded on the license to
practice medicine, the receiving authority shall be responsible for carrying
out the renewal or providing a written response stating the reasons where the
renewal is not carried out; where no written response is provided by the expiry
date recorded on the license to practice medicine, the license to practice medicine
shall continue to be in force as prescribed;
c) Where verification of
the practitioner's continuing medical education (CME) conducted by a foreign
authority or organization is required, the renewal period shall be 10 working
days from the date of receipt of the verification results.
3. The procedures for renewal of the license to practice
medicine for practitioners with the professional title of traditional medicine
practitioner, holder of a hereditary medicinal formula or hereditary treatment
method shall be carried out as follows:
a) The applicant for
renewal of the license to practice medicine shall submit an application as
prescribed in clauses 1 and 2 Article 26 of Decree No. 96/2023/ND-CP (in
person, by post or through electronic means) and pay fees and charges as
prescribed by law on fees and charges to the receiving authority at least 40
working days before the expiry date of the license to practice medicine;
Where the practitioner is
ill, injured or in a force majeure circumstance at the time of submission of
the renewal application, a written notice shall be sent to the receiving
authority to defer the submission of the renewal application for the license to
practice medicine;
The practitioner may
request deferral of the renewal date multiple times, but the total deferral
period shall not exceed 22 months from the expiry date of the license to
practice medicine;
b) During the period from
receipt of a complete application to the expiry date recorded on the license to
practice medicine, the receiving authority shall be responsible for carrying
out the renewal or providing a written response stating the reasons where the
renewal is not carried out; where no written response is provided by the expiry
date recorded on the license to practice medicine, the license to practice
medicine shall continue to be in force as prescribed.
Part 4. Application and
procedures for adjustment of the license to practice medicine
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a) The applicant for
adjustment of the license to practice medicine shall submit 1 set of documents
corresponding to each case prescribed in clauses 1 through 3 Article 136 of
Decree No. 96/2023/ND-CP (in person, by post or through electronic means) and
pay fees and charges as prescribed by law on fees and charges to the receiving
authority;
b) The receiving authority
shall adjust the license to practice medicine within 10 working days from the
date of receipt of a complete application; where the license to practice
medicine is not adjusted, a written response stating the reasons shall be provided;
The form of adjustment of
the license to practice medicine: a decision on adjustment of the scope of practice in
accordance with Form 10 Appendix I issued together with Decree No.
96/2023/ND-CP. The
decision on adjustment of the scope of practice shall form an integral part of
the issued license to practice medicine.
c) Where verification of
documents with foreign elements in the application for adjustment of the
license to practice medicine is required, the adjustment period shall be 10
working days from the date of receipt of the verification results.
2. From January 1, 2027, the procedures for adjustment of the
license to practice medicine for the cases prescribed in clause 1 Article 19 of
Decree No. 96/2023/ND-CP shall be carried out as follows:
a) The applicant for
adjustment of the license to practice medicine shall submit 1 set of documents
corresponding to each case prescribed in clause 1 or clause 2 Article 20 of
Decree No. 96/2023/ND-CP (in person, by post or through electronic means) and pay
fees and charges as prescribed by law on fees and charges to the receiving
authority;
b) The receiving authority
shall adjust the license to practice medicine within 10 working days from the
date of receipt of a complete application; where the license to practice
medicine is not adjusted, a written response stating the reasons shall be
provided;
The form of adjustment of
the license to practice medicine: a decision on adjustment of the scope of practice in
accordance with Form 10 Appendix I issued together with Decree No.
96/2023/ND-CP. The
decision on adjustment of the scope of practice shall form an integral part of
the issued license to practice medicine;
c) Where verification of
documents with foreign elements in the application for adjustment of the license
to practice medicine is required, the adjustment period shall be 10 working
days from the date of receipt of the verification results.
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1. Where a practitioner's license is suspended based on the
conclusion of the expert panel as prescribed in Article 101 of the Law on
Medical Examination and Treatment (point a clause 1 Article 34 of the Law on
Medical Examination and Treatment), the procedures for suspension of the
license to practice medicine shall be carried out as follows:
a) Where the expert panel
is established by the healthcare facility in accordance with point a clause 4
Article 101 of the Law on Medical Examination and Treatment:
- Within 5 working days from the date of the conclusion, the
President of the expert panel shall be responsible for signing and sending a
written notice to the healthcare facility;
- Within 5 working days from the date of receipt of the
written notice from the President of the expert panel, the healthcare facility
shall be responsible for submitting a written report to the health professional
authority under the province-level People's Committee, clearly stating the
reasons for the proposed suspension of the license to practice medicine;
- Within 5 working days from the date of receipt of the
written report from the healthcare facility, the province-level People's
Committee shall be responsible for issuing the suspension decision. The suspension decision
shall be based on the conclusion of the expert panel;
b) Where the expert panel
is established by the province-level People's Committee in accordance with
point b clause 4 Article 101 of the Law on Medical Examination and Treatment:
- Within 5 working days from the date of the conclusion, the
President of the expert panel shall be responsible for signing and sending a
written notice to the province-level People's Committee, clearly stating the
reasons for the proposed suspension of the license to practice medicine;
- Within 5 working days from the date of receipt of the
written request from the President of the expert panel as prescribed in point b
of this clause, the province-level People's Committee shall be responsible for
issuing the suspension decision. The suspension decision shall be based on the conclusion of
the expert panel.
2. Where a practitioner is suspended based on the conclusion of
a competent authority regarding professional ethics violations that do not
warrant revocation of the license to practice medicine (point b clause 1
Article 34 of the Law on Medical Examination and Treatment), the procedures for
suspension of the license to practice medicine shall be carried out as follows:
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- The competent authority shall send a written conclusion on
the professional ethics violations, including a request and clear reasons for
the suspension of the license to practice medicine, to the competent state
regulatory authority on health directly managing the practitioner;
- Within 5 working days from the date of receipt of the written
conclusion from the competent authority, the competent state regulatory
authority on health directly managing the practitioner shall be responsible for
issuing the decision on suspension of the license to practice medicine. The decision on suspension
of the license to practice medicine shall be based on the written conclusion of
the competent authority;
b) Where the competent
authority that concluded the practitioner has committed professional ethics
violations has the function of suspending or revoking the license to practice
medicine:
Within 5 working days from
the date of the written conclusion, the competent authority shall be
responsible for issuing the decision on suspension of the license to practice
medicine. The
decision on suspension of the license to practice medicine shall be based on
the written conclusion.
3. Where a practitioner is suspended due to insufficient health
to practice (point c clause 1 Article 34 of the Law on Medical Examination and
Treatment), the procedures for suspension of the license to practice medicine
shall be carried out as follows:
Within 5 working days from
the date of receipt of the written conclusion from the competent authority
(including: Court,
forensic assessment agency, health examination facility) that the practitioner
has insufficient health to practice, the competent state regulatory authority
on health directly managing the practitioner shall be responsible for issuing
the suspension decision. The suspension decision shall be based on the written
conclusion of the competent authority.
4. The decision on suspension of part or all of the scope of
practice of the practitioner shall include the following:
a) Suspension of part or
all of the scope of practice of the practitioner; where part is suspended, the
suspended scope shall be clearly stated;
b) Duration of suspension;
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d) Conditions for
resumption of practice.
5. Within 5 working days from the date of issuance of the
decision on suspension of part or all of the scope of practice of the
practitioner, the authority issuing the suspension decision shall be
responsible for:
a) Sending the suspension
decision to the practitioner and restricting the practitioner's scope of
practice on the health facility management information system, or sending it to
the healthcare facility where the practitioner works for implementation and to
the professional - social organization on medical examination and treatment for
oversight;
b) Sending the suspension
decision to the authority that issued the license to practice medicine to that
practitioner, where the authority issuing the suspension decision is not the
authority that issued the license to practice medicine.
6. Post-suspension handling shall be carried out in accordance
with Article 31 of Decree No. 96/2023/ND-CP.
Part 6. Application and
procedures for revocation of the license to practice medicine
A. Application
The application for
revocation of the license to practice medicine for the case prescribed in point
i clause 1 Article 35 of the Law on Medical Examination and Treatment shall
include:
1. Application form;
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B. Procedures
1. For cases prescribed in points a, b, c and d clause 1
Article 35 of the Law on Medical Examination and Treatment:
a) The agency,
organization or individual that discovers the practitioner falls within a case
requiring revocation of the license to practice medicine shall notify the
province-level People's Committee;
b) The province-level
People's Committee shall be responsible for verifying the application,
documents and information provided by the organization or individual; where the
case falls under revocation, a decision on revocation of the license to
practice medicine shall be issued.
2. For the case prescribed in point dd clause 1 Article 35 of
the Law on Medical Examination and Treatment:
The province-level
People's Committee shall be responsible for issuing a decision on revocation of
the license to practice medicine of the practitioner within 5 working days from
the date of receipt of the notification or service of process from the
competent authority regarding the practitioner falling within a case prohibited
from practicing in accordance with clauses 1, 2, 3, 4 and 6 Article 20 of the
Law on Medical Examination and Treatment.
3. For the case prescribed in point dd clause 1 Article 35 of
the Law on Medical Examination and Treatment:
a) Where the expert panel
is established by the healthcare facility in accordance with point a clause 4
Article 101 of the Law on Medical Examination and Treatment:
- Within 5 working days from the date of the conclusion, the President
of the expert panel shall be responsible for signing and sending a written
notice to the healthcare facility;
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- Within 5 working days from the date of receipt of the
written report from the healthcare facility, the province-level People's
Committee shall be responsible for issuing the decision on revocation of the
license to practice medicine. The revocation decision shall be based on the conclusion of
the expert panel.
b) Where the expert panel
is established by the province-level People's Committee in accordance with
point b clause 4 Article 101 of the Law on Medical Examination and Treatment:
- Within 5 working days from the date of the conclusion, the
President of the expert panel shall be responsible for signing and sending a
written notice to the province-level People's Committee, clearly stating the
reasons for the proposed revocation of the license to practice medicine;
- Within 5 working days from the date of receipt of the
written request from the President of the expert panel as prescribed in point b
of this clause, the province-level People's Committee shall be responsible for
issuing the decision on revocation of the license to practice medicine. The revocation decision
shall be based on the conclusion of the expert panel.
4. For the case prescribed in point h clause 1 Article 35 of
the Law on Medical Examination and Treatment:
Within 5 working days from
the date of receipt of the written conclusion that the practitioner has
committed professional ethics violations for the second time within the
validity period of the license to practice medicine, warranting suspension of
the license to practice medicine, from the competent authority, the competent
state regulatory authority on health directly managing the practitioner shall
be responsible for issuing the decision on revocation of the license to
practice medicine. The decision on revocation of the license to practice
medicine shall be based on the written conclusion of the competent authority.
5. For the case prescribed in point i clause 1 Article 35 of
the Law on Medical Examination and Treatment:
The receiving authority
shall issue a decision on revocation of the license to practice medicine within
10 working days from the date of receipt of the application for revocation of
the license to practice medicine submitted by the practitioner (in person, by
post or through electronic means).
6. The decision on revocation of the license to practice
medicine shall include the following:
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b) Decision on revocation
of the license to practice medicine and reasons for revocation;
c) Conditions for
resumption of practice.
7. Within 10 working days from the date of the revocation
decision, the revoking authority shall send the decision to the practitioner
and the healthcare facility where the practitioner works, and shall cancel the
practitioner's registration on the online portal or website of the receiving
authority and the health facility management information system.
APPENDIX IV
APPLICATION AND PROCEDURES FOR NEW
ISSUANCE, RE-ISSUANCE AND ADJUSTMENT OF HEALTH FACILITY OPERATING LICENSES
UNDER THE LAW ON MEDICAL EXAMINATION AND TREATMENT
(Issued together with Resolution No. 21/2026/NQ-CP dated April 29, 2026 of the
Government)
Part 1. Procedures for
re-issuance of the health facility operating license for private hospitals
1. A private hospital shall submit 1 set of documents for
re-issuance of the operating license as prescribed in Article 62 of Decree No.
96/2023/ND-CP and pay fees and charges as prescribed by law on fees and charges
to the competent authority for issuance of the operating license (hereinafter
referred to as the licensing authority).
2. Upon receipt of the application, the licensing authority
shall issue to the private hospital applying for re-issuance of the operating
license an acknowledgement of receipt.
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4. Within 3 working days from the date of receipt of the
written request for verification of information under clause 3 of this Part,
the Ministry of Health shall issue a written response verifying the information
in accordance with Form 02 issued together with this Appendix.
5. Within 4 working days from the date of receipt of the
Ministry of Health's verification document as prescribed in clause 4 of this
Part, or from the date of receipt of the application as prescribed in clause 2
of this Part in cases where the private hospital has submitted together with
the application the original operating license or a certified true copy thereof
as prescribed by law on certification of true copies from originals, the
licensing authority shall re-issue the operating license for the private
hospital in accordance with Form 03 issued together with this Appendix and
update information on the re-issuance of the operating license on its online
portal or website and on the health facility management information system. The decision on re-issuance
of the health facility operating license shall have the same legal effect as
the health facility operating license.
Part 2. Procedures for
adjustment of the health facility operating license for cases of change of
working hours or change of name or address of the healthcare facility without
change of location for private hospitals
1. Submit 1 set of documents for request to change name,
address or working hours of the healthcare facility as prescribed in clause 1
Article 64 of Decree No. 96/2023/ND-CP and pay fees and charges as prescribed
by law on fees and charges to the licensing authority.
2. Upon receipt of the application, the licensing authority
shall issue to the applicant an acknowledgement of receipt in accordance with
Form 02 Appendix I issued together with Decree No. 96/2023/ND-CP.
3. Where no amendment to the application is required, the
licensing authority shall send a written notice to the Ministry of Health for
verification of information of the private hospital applying for adjustment of
the operating license in accordance with Form 01 issued together with this
Appendix within 3 working days from the date recorded on the acknowledgement of
receipt under clause 2 of this Part, except where the private hospital has
submitted together with the application the original operating license or a
certified true copy thereof as prescribed by law on certification of true
copies from originals (the private hospital shall bear full legal
responsibility for the authenticity and validity of the certified true copy
from the original).
4. Within 3 working days from the date of receipt of the written
request for verification of information under clause 3 of this Part, the
Ministry of Health shall issue a written response verifying the information in
accordance with Form 02 issued together with this Appendix.
5. Within 4 working days from the date of receipt of the
Ministry of Health's verification document as prescribed in clause 4 of this
Part, or from the date of receipt of the application under clause 2 of this
Part in cases where the private hospital has submitted together with the
application the original operating license or a certified true copy thereof as
prescribed by law on certification of true copies from originals, the licensing
authority shall issue a decision on adjustment of the operating license due to
change of working hours or change of name or address of the healthcare facility
without change of location for the private hospital in accordance with Form 04
issued together with this Appendix.
6. Where amendment to the application is required, within 5
working days from the date recorded on the acknowledgement of receipt under
clause 2 of this Part, the licensing authority shall send a written notice to
the applicant specifying the documents and particulars requiring amendment.
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7. Upon receipt of the amended application, the licensing authority
shall issue to the applicant an acknowledgement of receipt in accordance with
Form 02 Appendix I issued together with Decree No. 96/2023/ND-CP for the
amended application:
a) Where the amended
application does not meet the requirements, the licensing authority shall send
a written notice to the applicant as prescribed in clause 6 of this Part.
Within 6 months from the
date of the licensing authority's written notice requesting amendments, the
applicant shall submit the amended application as required. After this period, where
the applicant fails to make amendments, or after 12 months from the date of the
initial submission where the amended application still does not meet the
requirements, the submitted application shall become invalid.
b) Where no further
amendments to the amended application are required, the licensing authority
shall proceed in accordance with clauses 3, 4 and 5 of this Part.
8. Within 5 working days from the date of issuance of the
decision on adjustment of the operating license, the licensing authority shall
publish and update on its online portal and on the health facility management
information system all information relating to the adjusted particulars.
9. The decision on adjustment of the health facility operating
license due to change of working hours or change of name or address of the
healthcare facility without change of location shall have the same legal effect
as the health facility operating license.
Form 01
SUPERVISING AGENCY/ORGANIZATION [1]
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SOCIALIST REPUBLIC OF VIETNAM
Independence - Freedom - Happiness
---------------
No. …/......[3]......
Re: request for
verification of operating license information of Hospital …[5]…
….[4]….., [date]…...
To: Ministry of Health.
On [month/day/year] ………[2]........ received the
application for re-issuance/adjustment of the health facility operating license
due to ……[6]…. from Hospital ……[5]......... with the following basic
information:
1. Hospital name: ……… [5]…………
2. Form of organization: ……… [7]……..
3. Operating address: …… [8]………
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5. Issued operating license number: ………….
6. Date of issuance of operating license: ………………
………[2]…….. respectfully
requests the Ministry of Health to confirm the authenticity of the above
information as the basis for re-issuance/adjustment of the health facility
operating license for Hospital ……[5]……..
Yours sincerely.
Recipients:
- As above;
………………
- Filed: ……..
TITLE OF SIGNATORY
(Signature, full name and seal)
____________________
[1] Name of the direct supervising agency or organization of the
licensing authority (if any).
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[3] Abbreviated name of the licensing authority.
[4] Location.
[5] Name of the private hospital applying for
re-issuance/adjustment of the health facility operating license (note: state the full name
including the parent company, e.g., Hospital A under Joint Stock Company B).
[6] State the case for re-issuance or adjustment of the health
facility operating license under the cases prescribed in clause 1 Article 53
and points c and d clause 1 Article 54 of the Law on Medical Examination and
Treatment; specifically for re-issuance due to information errors or adjustment
of the operating license due to change of working hours or change of name or
address of the healthcare facility without change of location, clearly state
the erroneous or adjusted content.
[7] Form of organization on the issued operating license.
[8] Operating address on the issued operating license.
[9] Daily working hours on the issued operating license.
Form 02
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SOCIALIST REPUBLIC OF VIETNAM
Independence - Freedom - Happiness
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No. …/......[11]......
Re: verification of
operating license information of Hospital …[12]…
Hanoi, ………….[date]
To: ……[13]……
On [month/day/year] ………[1]…….. received
Official Letter No. ……[14]….. from …….[4]……. regarding the request for
verification of operating license information of Hospital ……[3]……. Upon reviewing the
Official Letter, ………..[1]......... provides the following response:
The information of
Hospital ……...[3]......... is/is not consistent with the health facility
operating license issued by the Ministry of Health [15].
The above is the response
of ………[1]…….. to …….[4]……. as the basis for re-issuance/adjustment of the
health facility operating license for Hospital ……[5]……..
Yours sincerely.
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Recipients:
- As above;
…………
- Filed: ……..
TITLE OF SIGNATORY
(Signature, full name and seal)
_____________________
[10] Name of the former licensing authority (Department of
Medical Examination and Treatment Management or Department of Traditional
Medicine and Pharmacy Management).
[11] Abbreviated name of the licensing authority.
[12] Name of the private hospital applying for
re-issuance/adjustment of the health facility operating license (note: state the full name including the parent company, e.g., Hospital A under Joint Stock Company B).
[13] Name of the authority requesting verification of health
facility operating license information.
[14] Number of the Official Letter requesting verification of
operating license information.
[15] Where the content is not consistent with the operating license
issued by the Ministry of Health, clearly state the discrepancies.
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Form 03
SUPERVISING AGENCY/ORGANIZATION [16] NAME OF
AGENCY/ORGANIZATION [17]
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SOCIALIST REPUBLIC OF VIETNAM
Independence - Freedom - Happiness
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No. …/......[18]......
….[19]….., [date]…...
DECISION
On
re-issuance/adjustment of the health facility operating license
……[20]……
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Pursuant to Decree No. 96/2023/ND-CP
dated December 30, 2023 of the Government elaborating on certain articles of
the Law on Medical Examination and Treatment;
Pursuant to Resolution
No. /2026/NQ-CP dated … 2026 of the Government on reduction and simplification
of business conditions, administrative procedures and delegation of authority
to administer administrative procedures in the health sector;
Pursuant to the
application for re-issuance/adjustment of the health facility operating license
dated … month …. year… of .…[21] ….
At the proposal of
............... [22]..........
HEREBY DECIDES:
Article 1. Re-issue/adjust the health facility operating license due to
……[23]…. for:
1. Name of healthcare facility: ………[6] …………
2. Form of organization: ……… [24]……..
3. Operating address: …… [25]………
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Article 2. This Decision comes into force from the date of signing and
shall replace operating license No. …[27]…/BYT-GPHD issued by the Minister of
Health on ……[28]…...
Article 3. The individual named in Article 1 and ... [29]... shall implement this Decision.
Recipients:
- As per
Article 3;
………..…
- Filed: ……..
TITLE OF SIGNATORY
(Signature, full name and seal)
_____________________
[16] Name of the direct supervising agency or organization of the
licensing authority (if any).
[17] Name of the licensing authority.
[18] Abbreviated name of the licensing authority.
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[20] Title of the head of the licensing authority.
[21] Name of the private hospital applying for
re-issuance/adjustment of the health facility operating license (note: state the full name including the parent company, e.g., Hospital A under Joint Stock Company B).
[22] State the title of the head of the unit assigned the focal
function for re-issuance and adjustment of the health facility operating
license.
[23] State the case for re-issuance or adjustment of the health
facility operating license under the cases prescribed in clause 1 Article 53
and points c and d clause 1 Article 54 of the Law on Medical Examination and
Treatment.
[24] Form of organization on the issued operating license.
[25] Operating address of the healthcare facility.
[26] Daily working hours of the healthcare facility.
[27] Number of the previously issued operating license of the
private hospital.
[28] Date of issuance of the previous operating license of the
private hospital.
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