Public Consultation On Implementation Of Bioequivalence (BE) Study Requirements For New Drug Products Containing Scheduled Poison

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Online public engagement is in line with the government's aspiration to support the principles of transparency and equality for the implementation of a law.

Therefore, this page is available for public consultation and will present new proposals or amendments to the draft law (including laws, policies, regulations, etc.). The draft will appear on this page for a period of 14 working days.

The public is encouraged to provide comments and views on the National Pharmaceutical Regulatory Agency (NPRA), Ministry of Health Malaysia during this period.

 

 

Feedback/Comment Period : 16/04/2019 - 15/05/2019

 

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1. Public Consultation On Implementation Of Bioequivalence (BE) Study Requirements For New Drug Products Containing Scheduled Poison Download

 

 

Feedback/Comment Form

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1. Comment Form Download

Please email the filled table to Dr Yvonne Khoo ( Alamat emel ini dilindungi dari Spambot. Anda perlu hidupkan JavaScript untuk melihatnya. ) by 15 May 2019. 

Thank you for taking time to assist in our efforts towards process improvement.

 

National Pharmaceutical Regulatory Agency (NPRA)
Lot 36, Jalan Universiti, 46200 Petaling Jaya, Selangor, Malaysia.
  • Email: npra@npra.gov.my
  • Phone: +603-7883 5400
  • Fax: +603-7956 2924, +603-7956 7075

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  • Last Modified: Khamis 12 September 2019, 14:20:55.
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