Advanced certification program provides training in cutting-edge regulatory tools and technologies essential for the pharmaceutical and life sciences industries.

Designed for aspiring regulatory professionals and medical writers, this program enhances technical competency and regulatory acumen for efficient document management, data analytics, and regulatory submissions.

Participants will gain expertise in top industry standard platforms like Adobe Acrobat, Office 365, and Veeva Vault along with insights into AI & ML.

This course covers regulatory tools, structured product labelling, and product lifecycle management tools ensuring proficiency in global compliance standards.

Learners will also work with eValidators, SPOR and CTIS gaining practical experience in clinical trial submission systems.