The Company’s regulatory practices are well defined by a team of Qualified Pharmacists, headed by a Medical Doctor and a Senior Regulatory Manageress. The operations handled by this Division include registration of Products, Product Licensing and Post Marketing issues amongst others.

Evaluation of Dossiers on given guidelines prior to submission to the National Medicines Regulatory Authority (NMRA) and liaising with regulatory departments of the respective manufacturers represented by the company to complete the dossiers, is a priority area of the Division. In addition, constant monitoring of the processes adopted by the Warehouse Personnel in adhering to specifics with regard to storage and distribution of pharmaceutical preparations marketed by the Company too is considered a key activity area.

In line with several agreements signed by the Company with partners worldwide, the Regulatory Team is assigned the responsibility of pharmacovigilance and adopts CIOMS guidelines.