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Procedure NameGranting permission to import drugs/medicines for clinical trials
Description
Category
License/Permit
Responsible Agency                   
 
Drug Administration of Vietnam - Ministry of Health
Address:                             
Phone:
Email:
Legal base of the Procedure
  • Law on Pharmacy No. 105/2016/QH13
  • Decision 151/2007/QD-TTg dated September 12, 2007, promulgating the Regulation on the Import of Drugs without Registration Numbers in Vietnam
  • Circular 47/2010/TT-BYT dated December 29, 2010 of the Ministry of Health guiding the export, import of drugs/medicines and packaging in direct contact with drugs/medicines
Processing time
  • Within 15 working days from the date of reception of adequate and valid dossier
Fee
VND 0
 
Required documents:
No
Type of documents
Note
1
Import order (Forms 11a, 11b, 11c)
01 original copy
2
The research plan of clinical trials approved by the Minister of Health
01 original copy
 
Process Steps
Step 1
 
The applicant shall submit a dossier of Application to the Drug Administration of Vietnam - Ministry of Health
Step 2
The Drug Administration of Vietnam shall receive and examine the dossier.
Step 3
The Administration shall inform the applicant of the results.
In case of refusal, the Administration shall reply in writing and clearly state relevant reasons.
 
Process Map:
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This procedure apply to theses Measures.
namedescription
Importing drugs for clinical trial purposesImporting drugs for clinical trial purposes