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Department of Pharmaceutical Regulatory Affairs
About The Department
Department of Pharmaceutical Regulatory Affairs at SRM College of Pharmacy, SRM Institute of Science and Technology, is dedicated to preparing future leaders in pharmaceutical regulation through our comprehensive academic programs, cutting-edge research, and strong industry connections. Our curriculum includes Master’s, and Ph.D. degrees, along with professional certifications, all 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 the industry ensure that our students have access to valuable internships, job placements, and networking opportunities. Graduates from our department are highly sought after and well-prepared for a variety of careers in the pharmaceutical industry. Our alumni have gone on to become Regulatory Affairs Specialists, Compliance Officers, Clinical Trial Managers, and Regulatory Policy Analysts, among other roles. They are 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.
Pharmaceutical Regulatory Affairs
Dr.R.Kamaraj
HOD
Welcome message
Regulatory Affairs in a 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, supervising-writing / 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 in first semester. In second semester students will learn marketing registration of Drugs and Cosmetics, Herbal and Biological, Medical Devices and Nutraceuticals to various regulatory agencies across the world. In third semester the learning activities are Research Methodology, Biostatics, Research proposal presentation and participating in journal club. Fourth semester students will carry out their project in the pharmaceutical industry.
Faculty
Teaching environment and quality are central to SRMIST’s capabilities profile. Our Professors are the reason for our continued ability to foster vibrant and value adding learning experiences for our students. The success of our students’ in terms of their learning and overall development enabled by our faculty members is an area of focus of Leadership at SRMIST. Many opportunities are provided to our faculty members to conduct research and engage with the industry in consultancy and other projects. This platform brings to our faculty members an opportunity to expand their knowledge contribution as well as bring those rich experiential inputs to the classrooms and labs therefore benefiting our students.
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