This 3-month intensive certification program equips professionals with essential knowledge and practical skills in Regulatory Affairs, Clinical Research, and Medical Writing. Covering key areas like Drug Discovery & Development, Clinical Trial Applications, and Regulatory Intelligence, the course ensures a strong foundation in global regulatory frameworks.

Participants will gain expertise in Regulatory Writing, CMC (Chemistry, Manufacturing & Controls), GxP Compliance, Submission Publishing, and Life Cycle Management, along with hands-on training in Labelling & Artwork Management, RIMS (Regulatory Information Management Systems), and Supply & Product Management.

Ideal for aspiring regulatory professionals, medical writers, and life sciences experts, this program enhances career opportunities in pharmaceuticals, biotechnology, and healthcare sectors.