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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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
12593 – – Containing quinine sulphate or bisulphate, of a kind taken orally
12594 – – Containing quinine or its salts or other antimalarial substances, other than goods of subheading 3004.40.20 or 3004.40.30
12595 – – Containing papaverine or berberine, of a kind taken orally
12596 – – Containing theophyline, of a kind taken orally
12597 – – Containing atropine sulphate
12598 – – Other
12599 – – Of a kind suitable for children, in syrup form
12600 – – Other, containing more than one vitamin: – – – Of a kind taken orally
12601 – – Other, containing more than one vitamin: – – – Other
12602 – – Other: – – – Containing vitamin A, B or C
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