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Peringatan: Pelaksanaan Kawalan Regulatori Bahan Aktif Farmaseutikal (API) Untuk Produk Yang Tamat Tempoh Pendaftaran Mulai 1 Januari 2020

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  1. Direktif BPFK/PPP/01/03/J3(11) bertarikh 27 Jun 2014 adalah dirujuk.
  2. Garispanduan untuk prosedur kawalan regulatori API boleh didapati di Guidance Notes Required Documents for API Information Version 2.0
  3. Carta aliran untuk kawalan regulatori API ke atas produk berdaftar (yang mengandungi racun berjadual) boleh dirujuk.
  4. Borang permohonan Form RegA1 (Application Form for Section S Revision for Product Registered Before the Implementation of Directive on Regulatory Control of API) akan berkuatkuasa mulai 1hb Oktober 2018. Borang ini boleh didapati di laman web NPRA (Garispanduan-API).

 

National Pharmaceutical Regulatory Agency (NPRA)

Lot 36, Jalan Universiti (Jalan Prof Diraja Ungku Aziz), 46200 Petaling Jaya, Selangor, Malaysia.

  • Phone: +603-7883 5400

 

 

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The Government of Malaysia and the National Pharmaceutical Regulatory Agency are not responsible for any loss or damage caused by the usage of any information obtained from this website.

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  • Last Modified: Thursday 19 September 2024, 16:35:40.

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