Regulatory affairs IPR & Patents Course

Overview

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.

Minimum Education