Recommendations from the GMP Workshop 2017

April 7th, 2017

A workshop for medicinal product manufacturers to promote Regulatory compliance on Good Manufacturing Practice(GMP) was conducted from 31March -2 April 2017. Please click on the link below to view the recommendations:
Regulatory Notification on mandatory submission of testing report for ethylene glycol and diethylene glycol in oral liquid preparations.

June 26th, 2024
Competency Examination on 10 May, 2024

April 26th, 2024
Competency Examination on 11 March, 2024

February 27th, 2024
Notification On Revised Client Visiting Hours For Enhanced Service Delivery

February 7th, 2024
Regulatory Notification on requirement of Import Authorization for prioritized list of medical devices

February 5th, 2024
Regulatory Notification On Revised Document Requirement For Medical Devices Registration

January 25th, 2024