Publication | Open Access
Comparison of Regulatory Requirements for Registration of Pharmaceutical Drugs in Asean and GCC Regions
11
Citations
7
References
2019
Year
Product RegistrationRegulatory ApprovalDrug ManufactureGlobal HealthPharmacoepidemiologyPharmacologyProcess Analytical TechnologyDrug Product RegistrationPharmacotherapyIch Ctd FormatPharmaceutical DrugsGcc RegionsRegulatory HarmonizationRegulatory ConsiderationMedicineRegulationDrug DiscoveryRegulatory Requirements
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.
| Year | Citations | |
|---|---|---|
Page 1
Page 1