Snehal M.

Seasoned professional having 8 years of experience in the domain of Drug Regulatory Affairs. Accountable for life cycle management of the products in Regulated, Semi-regulated and row market. Accountable for delivery of assigned submissions to agreed timeframes and appropriate content independently and confidently for EU and Rest of the World (ROW) market. Responsible for the coordinating the maintenance activities associated with an approved product, including product renewals, label harmonization, Site Registrations/Site Renewals, Tenders, Variations etc. Attended the Bio-equivalence dosing audits and involved in preparation and compilation of Module 4 and module 5. Ensure compliance with all relevant regulatory guidelines and support other functional areas as needed.