Pharmaceutical Regulatory Affairs

Department of Pharmaceutical Regulatory Affairs

The Department of Pharmaceutical Regulatory Affairs at MVM College of Pharmacy aims to prepare future leaders in pharmaceutical regulation through our comprehensive academic programs, cutting-edge research, and strong industry connections. Our curriculum includes Master’s designed to provide an in-depth understanding of regulatory policies, drug development, and compliance strategies. Our faculty members are seasoned professionals with extensive industry experience, bringing a wealth of real-world knowledge and academic expertise to the classroom. They are dedicated to mentoring students and equipping them with the skills needed to excel in the complex field of pharmaceutical regulation. Our academic programs cover a broad spectrum of topics, from the fundamentals of regulatory affairs to advanced concepts in drug safety, efficacy, and marketing approval processes. Our strong ties with industry ensure that our students have access to valuable internships, job placements, and networking opportunities. Graduates from our department will be highly sought after and well-prepared for a variety of careers in the pharmaceutical industry such as Regulatory Affairs Specialists, Compliance Officers, Clinical Trial Managers, and Regulatory Policy Analysts, among other roles. They will be known for their thorough understanding of regulatory frameworks, their ability to navigate complex compliance issues, and their commitment to ensuring the safety and efficacy of pharmaceutical products.

Overview

Regulatory Affairs in the pharmaceutical industry, is a profession which acts as the interface between the pharmaceutical industry and Drug Regulatory authorities across the world. Play a very important role in the journey of a product from laboratory to pharmacy shop. Regulatory Affairs is a unique mixture of science and management to achieve a commercially important goal within a drug-development organization. Regulatory Affairs takes care of development plan, supervisingwriting / reviewing and assembling and submission management. This course is designed to impart fundamental knowledge on Good Regulatory Practices, Documentation and Regulatory Writing, Clinical Research Regulation and Intellectual Properties Rights, marketing registration of Drugs and Cosmetics, Herbal and Biological, Medical Devices and Nutraceuticals to various regulatory agencies across the world.

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