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.

Resources

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Procedures


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

This measure applies to commodity/s


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
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