This comprehensive 3-month certification program provides in-depth training in Clinical Research, Pharmacovigilance, and Medical Writing, equipping participants with industry-relevant skills. Designed for aspiring professionals, the course covers key aspects of clinical trial management, drug safety regulations, adverse event reporting, regulatory documentation, and scientific writing. Led by industry experts, the program includes interactive sessions, case studies, and hands-on assignments. Participants will undergo periodic assessments to evaluate their proficiency and receive a certification upon successful completion. Ideal for graduates and professionals seeking career advancement in the pharmaceutical, healthcare, and research sectors.