REGULATORY AFFAIRS PROGRAMMES (Approved by Quality Council of India (QCI), Government of India)

IGMPI's another addition to the hat of Online programmes is comprehensive, interactive and intelligently structured Post Graduate, Executive Diploma and Industry Certificate Programmes in Regulatory Affairs; targeting demand and supply disproportion of the Pharmacautical, Medical Devices and Food industries. From products, to processes, documentation to services, research to testing, manufacturing to packaging; all aspects of the industry are guarded by set of Govt. regulations. The legislations are carved to set a streamlined and safest path for products from company to the market and then to the consumer. Thus rules are important and customer safety is a reason sufficient enough to comply with the guidelines.

Federal Govt. (especially healthcare authorities like FDA and WHO) and Govt of India have set laws and regulations when it comes to drugs, medical devices and food reaching the customers. To update the knowledge, training into good practice and compliance for regulations, audit, check and review compliance with regulations, accomplishing appropriate documentation of varied activities being conducted at a manufacturing plant, food processing unit, medical device manufacturing, Bio technology laboratory or manufacturing unit or any other organization or unit of the the said industries, a well-trained division of regulatory affair professionals is a must. IGMPI thus, proposes to make available regulatory affairs knowledge, training, practical tips, case studies and all the needed stuff through an interactive online programmes. The study resources and online live classes and certification exams all tend to motivate and make ready regulatory affairs professionals with expertise in the field, to better serve the industry.

These online programmes as well as regular classroom programmes have following tempting features which are definite to benefit one to all participants of the Programme:

• - Comprehensive information, clearly targeting the Pharma, Medical Devices and Food industries in the respective programmes;
• - Well-structured programme, intelligently put together under guidance of industry experts from same field;
• - Easy to use, browse and explore e-tools woven remarkably well into the programme make the study material, lectures, online database, examination preparation modules as well as assessment papers easily accessible.
• - Live Interactive classes in Online modes and online exams make things easier and less complicated for the students and industry participants

Drug Regulatory Affairs

Pharmaceutical Regulatory Affairs (12 months)
Pharmaceutical Regulatory Affairs (6 months fast track)
Pharmaceutical Regulatory Affairs (3 months fast track)
Certificate in Registration of Drug and Dossier Preparation (CTD and e CTD Submission) (3 months)
Certificate in Drug Registration (European Market) (3 months)
Certificate in Drug Registration (GCC Countries) (3 months)
Certificate in Drug Registration (African Countries) (3 months)
Certificate in Drug Registration (India) (3 months)
Certificate in Drug Registration (US MARKET-ANDA, NDA etc.) (3 months)
Certificate in Preparation and Submission of Drug Master File (DMF) (3 months)
Certified Drug Regulatory Affairs Professional

Medical Devices Regulatory Affairs

Regulatory Affairs (Medical Devices) (12 months)
Regulatory Affairs (Medical Devices) (6 months fast track)
Regulatory Affairs (Medical Devices) (3 months fast track)
Certificate in European Union (EU) Medical Devices Regulation (3 months)
Certificate in EU IVD Medical Device Regulation (3 months)
Certificate in Medical Devices Directive, CE Marking for Europe (93/42/EEC) (3 months)
Certificate in In Vitro Diagnostic Medical Device Directive – CE Marking for Europe (98/79/EC) (3 months)
Certified Medical Device Regulatory Affairs Professional

Food Regulatory Affairs

Food Regulatory Affairs (12 months)
Food Regulatory Affairs (6 months fast track)
Food Regulatory Affairs (3 months fast track)
Certified Food Regulatory Affairs Professional

Food Intellectual Property Rights

Intellectual Property Rights (12 months)
Intellectual Property Rights (6 months fast track)
Intellectual Property Rights (3 months fast track)

Regulatory Toxicology

Regulatory Toxicology (12 months)
Regulatory Toxicology (6 months fast track)
Regulatory Toxicology (3 months fast track)

Intellectual Property Rights

Intellectual Property Rights (12 months)
Intellectual Property Rights (6 months fast track)
Intellectual Property Rights (3 months fast track)

Programme Fee Details

How to apply

Pharmaceuticals | Food | Clinical Research | Healthcare | Medical Coding | Medical Device | Nanotechnology | IPR

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