Name | Registration requirement of pharmaceutical manufacturer for importers or representative offices |
Description | Drug Import companies and representative offices shall firstly be registered for pharmaceutical manufacturing just being approved to be registered of Drug productions in the Ministry of Health. |
Comments | To ensure good manufacturing practice in drug production and to ensure that the drug productions are of high quality agreeing to the international standards |
Validity From | 01/08/2013 |
Validity To | 31/12/9999 |
Reference | |
Technical Code | P15 |
Agency | Ministry of Health |
Created Date | 2023-03-08 06:17:03 |
Updated Date | 2023-03-08 06:17:03 |
Status | publish |
Measure Type | Registration Requirement |
Legal/Regulation | Prakas No. 003 on the Procedures and Conditions of the Submission of the registration of Pharmaceutical Manufacturer from Overseas |
Un Code | 2180-Export Prohibition |
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Procedure Name | Description | Category | View Procedure Detail with Relevant Forms |
---|---|---|---|
Application for Registration of Pharmaceutical Manufacturer from Overseas | Procedure to obtain a Certifcate for Pharmaceutical Manufacturer from Overseas | View |
HS Code | Description |
---|---|
12583 | – – Containing tetracyclines or chloramphenicols or derivatives thereof: – – – Other |
12584 | – – Other: – – – Of a kind taken orally or in ointment form |
12585 | – – Other: – – – Other |
12586 | – – Containing insulin |
12587 | – – – Containing dexamethasone or their derivatives |
12588 | – – – Containing hydrocortisone sodium succinate or fluocinolone acetonide |
12589 | – – – Other |
12590 | – – Other |
12591 | – – Containing morphine or its derivatives, for injection |
12592 | – – Containing quinine hydrochloride or dihydroquinine chloride, for injection |