Applied Clinical Research, Clinical Trials and Regulatory Affairs

Author(s): Mohit, Aakash Deep*, Gaurav Khurana, Jagdeep Kumar and Akshay Monga

DOI: 10.2174/2213476X06666190128145525

Cite As
Comparison of Regulatory Requirements for Registration of Pharmaceutical Drugs in Asean and GCC Regions

Page: [62 - 70] Pages: 9

  • * (Excluding Mailing and Handling)

Abstract

Background: The product registration in rest of the world is a challenging task because they are not harmonized. ASEAN and GCC regions come under semi-regulated market. These regions have somewhat harmonized their regulatory organization. The significance of an emerging market is increasing globally. It is important for pharmaceutical companies to be up-to-date with the latest regulatory development. ASEAN used ACTD format and GCC used ICH CTD format for drug product Registration. ASEAN includes a group of countries like Singapore, Philippines etc. Whereas GCC includes Bahrain, Kuwait, Oman, Qatar, Saudi Arabia and UAE.

Conclusion: This review article focuses on general regulatory requirements of registration of pharmaceuticals in ASEAN and GCC region.

Keywords: Regulation, ASEAN, GCC, pharmaceutical companies, drugs, guidelines.