NPRA Banner

               
Product Search   QUEST3+ System   Enquiries   Sitemap  

Bioequivalence

Guidelines on Bioequivalence

Malaysia has fully adopted ASEAN guideline since March 2015 and it is the most current guide for the conduct of bioequivalence studies. This guideline is adopted from the Guideline on the Investigation of Bioequivalence” (European Medicines Agency, London, 20 January 2010, CPMP/EWP/QWP/1401/98 Rev 1) with some adaptation for ASEAN application.

ASEAN Guideline for the Conduct of Bioequivalence Studies, March 2015

This guideline is to be read in conjunction with all relevant directives, circulars and updates regarding bioavailability and bioequivalence studies.

In addition, other relevant and latest international guidelines e.g. by EMA, USFDA, ICH should also be referred to complement the ASEAN Guideline. 

 

National Pharmaceutical Regulatory Agency (NPRA)

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

  • Phone: +603-7883 5400

 

 

DISCLAIMER

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.

Site Last Modified

  • Last Modified: Selasa 03 Disember 2024, 10:01:04.

Search

Menu Utama