Frequently Asked Question

30. What are the guidelines for inspection of manufacturing plants?

The MCAZ conducts inspections in line with current WHO GMP guidelines. Upon submission of an application of a medicine with the Authority, the manufacturer should request for inspection of their site through email: and the request should be accompanied with an updated site master file and list of products submitted for registration. A pro forma invoice will hence forth be issued and dates for inspection will be scheduled upon receipt of payment for the inspection.