Regulatory Affairs

Regulatory Affairs team collect & evaluate data generated by R & D dept. Our Regulatory affairs team is having potential to prepare regulatory document as per Country guidelines/ ACTD/ CTD format for submission in Non Regulated, Semi Regulated and Regulated country.

Our Regulatory Affairs is involved in preparing and submitting the relevant regulatory dossiers to health authorities. Regulatory Affairs is dynamically involved in every stage of development of a new medicine.

Our Regulatory Affairs team keeps track of the ever-changing legislation in all the regions in which the company intends to market its products.