The Certificate Course in Drug Regulatory Affairs is a specialized program focused on providing participants with in-depth knowledge and skills related to the regulatory requirements and processes specific to generic drug approval in the United States (Regulated Market). This course will cover the regulations set forth by the U.S. Food and Drug Administration (FDA) for Abbreviated New Drug Applications (ANDAs) and equip participants with the expertise needed to navigate the complex landscape of generic drug development, submission, and compliance. Course Details: - All recorded lectures & content are available in the course content section. - Course content validity for Three Years. - Certificate validity Lifetime. - Students Eligibility: Any Life science candidates/ B.Pharm/ M.Pharm etc. - Course Maximum Duration: 2 months - Course completion Certificate to be issue after two months from registration date. - If Anyone need earlier Certification before two months, they should go through a Personal Interview and test series. - They Should message in Application 💬 for the urgent certification. - we are not providing jobs through our academy but guiding students to right direction. Upcoming Live Classes Every Sunday @8PM For any time, any query please contact 📧defineacademyindia@gmail.com 🪀+91 63706 70196