I’m a Regulatory Affairs Specialist with hands-on experience in Pakistan’s pharmaceutical compliance landscape, particularly in working with DRAP regulations, CTD dossier preparation, and Health & OTC product enlistment. Over the years, I’ve helped manufacturers, importers, and professionals navigate the complex regulatory framework by providing practical support in document submissions, DRAP portals, and SOP development.

My mission is to simplify Drug Regulatory Affairs for learners, whether you're a student, pharmacist, QA/QC officer, or regulatory consultant. This course is designed to provide not just theoretical understanding, but also real-world application — including official DRAP forms, checklists, and case-based training.

Join me to gain career-ready regulatory skills and confidently manage licensing, registration, and compliance in Pakistan’s growing health and pharma sector.