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Regulatory affairs IPR & Patents

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Regulatory affairs courses in India

Regulatory affairs (RA), also called government affairs, are a profession within regulated industries, such as pharmaceuticals, medical devices, energy, and banking. Regulatory affairs also have a very specific meaning within the healthcare industries globally and professionals can be recruited in Pharma companies, medical devices, biotech, biologics and functional food areas. It deals with government or law. Global regulatory agencies are as USFDA (United States Food and Drug Administration) and European Union of Drug Regulatory Affairs (EUDRA).
Course Objectives: The GIHS Program is developed to prepare professionals for regulatory affairs positions in the pharmaceutical, biopharmaceutical and medical device industries i.e. to facilitate them with the educational foundation that will support them advance in the regulatory affairs profession. The program will provide the students with the fundamentals required in both regulatory affairs and quality operations. This course is designed to give industry level education in field of legal and regulatory issues. The program focuses on regulatory affairs concept which the Pharma companies must comply to sell their drugs both domestically and in the international market. Pharmaceutical regulatory affairs courses in Healthcare Industry is related to IPR (Intellectual Property Rights), Patents, copyrights and Trademarks with quality standards. We provide degree certified regulatory affairs courses, IPR certificate course in India.
Eligibility: All Science Graduates, MBBS, BDS, BHMS, BAMS, BPT, BUMS, B. Pharm, M. Pharm, Pharmacy, Occupational Therapist, B.Sc., M.Sc., Life science, Medical Laboratory, Nursing, Microbiology, Biomedical, Biotech and all professionals working with Hospitals & Healthcare Organizations.
Mode or Methodology: Online & Distance Learning
Examination: Online & Distance Exams (MCQ / Theoretical) / Projects
Placement Assurance: Successful candidates would get the placement support. CVs of successful candidates would be forwarded to various Organizations.
Certification: GIHS Certificate would be awarded to only successful candidates.

Career Options

  • Regulatory affairs manager

    Oversees the company’s production activities and ensures compliance with applicable regulations and standard operating procedures.

  • Regulatory affairs specialist/ Compliance specialist

    They assist in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. They are often employed by pharmaceutical, biotechnology...

Gihsonline Advantage

GIHS provides the best courses helps you to get the start up in the healthcare field. These courses are ad-hoc to your professional career and provide you the additional benefit to be the part of an organization.









Fees, Payment & Program Duration

Certificate 3 Months- 22000/- INR & Fees for International Candidates – 450$ USD

Post Graduate Diploma Program (One Year) – 32000/- INR & Fees for International Candidates – 699 $ USD

Fast Track PG Diploma Program (4 Months) – 36000/- INR & Fees for International Candidates – 750 $ USD

Cheque / Demand Draft/Cash in the name of “Global Institute of Health Science”

Online Transfer through NEFT or RTGS

Fee can also be deposited in GIHS bank account (For more details Click Here).

Disclaimer: This course details are for the purpose of awareness about the program and career opportunities.

The exact information on course structure may vary from this information.

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  • This Arshad Hussain, Working with TASNEE company on the position of Senior Specialist- Laboratory & QA/QC. I did PGDRA course from GIHS. The materials provided by GIHS to cover the PGDRA course was sufficient to understand & getting well skilled about Regulatory Affairs.. I am very thankful to GIHS & their coordinators for their cooperation & well communication during the course.


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  • Dear Sir, I learned a lot about my course "Regulatory affairs". Thank you for your support and encouragement to get the best results in the exam at the end of course. Thank & regards, K.M.Subrahmanyam.


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    Clinical Research (Ethics Committee)

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Frequently Asked Questions

While the specifics may depend on different factors, generally regulatory affairs professionals are well-compensated. This is because of the critical role they play in ensuring compliance with regulations and facilitating the approval of products.
The role of regulatory affairs involves ensuring that products comply with regulatory requirements, especially in industries like pharmaceuticals, biotechnology, and medical devices.
Yes, there is significant scope for regulatory affairs professionals, especially in industries like pharmaceuticals and healthcare. As regulatory requirements continue to evolve, companies are looking for professionals who can help them abide by complex regulations.
IPR or intellectual property rights in the pharma industry are crucial for protecting innovations, inventions, and proprietary knowledge related to drugs and healthcare products. Professionals in the field play a key role in securing patents, trademarks, and copyrights.
Yes, IPR is a promising career in India, especially in industries like pharmaceuticals where innovation and protection of intellectual property are critical. With the increasing emphasis on research and development, the demand for professionals with expertise in IPR, including patent agents and attorneys, is growing in India.

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