This 2-month certification program provides hands-on training in cutting-edge regulatory tools and technologies essential for the pharmaceutical and life sciences industries. Participants will gain expertise in industry-standard platforms like Veeva, Adobe Acrobat, Office 365, and Power BI, along with insights into Artificial Intelligence applications in regulatory affairs.

The course covers Structured Product Labelling, Regulatory Intelligence, and Product Lifecycle Management (PLM) Portals, ensuring proficiency in global compliance standards. Learners will also work with Lorenx eValidator, SPOR, IDMP, DADI, and Eudra Vigilance, gaining practical experience in clinical trial submission systems like CTIS.

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