REGULATORY AFFAIRS

The registration of new products is carried out by our in-house Regulatory Affairs Department headed by a qualified pharmacist. The Regulatory Affairs Department handles all stages of the registration procedure, from initial review of the files through submission, including constant updates.

This arrangement has resulted in a rapid turn around time for registration for NCE's and other products submitted.

Our expertise includes registration of both biological and chemical pharmaceuticals, in addition to nutritional products, cosmetics and medical devices.

Pharmacovigilance is the responsibility of this department and ensures full compliance with local regulations and procedures. We co-operate with our overseas partners so that the data flow necessary for reporting is carried out in a timely and efficient manner.