Name | Registration requirement of pharmaceutical manufacturer for exporter |
Description | Drug export companies shall firstly be registered of pharmaceutical manufacturers just being approved to be registered of Drug productions in the Ministry of Health. |
Comments | To receive the correct information provided by pharmaceutical manufacturers about the good manufacturing practice situation in drug production to ensure that the drug productions are high quality agreeing to the international standard. |
Validity From | 01/08/2013 |
Validity To | 31/12/9999 |
Reference | Article 2, 3, 4, 6 |
Technical Code | P69 |
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 | 2320-Export technical measures, n.e.s. |
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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 |