Institute of Good Manufacturing Practices India

  • Institute of Good Manufacturing Practices India
  • Global accredited training & certification provider
  • Approved by Quality Council of India (QCI) & Accredited Vocational Institution of Ministry of HRD, Government of India
  • Approved Training Institute of Food Safety and Standards Authority of India (FSSAI)
  • Recognized by Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India
  • An ISO 9001:2015 Certified Organisation registered under The Societies Registration Act,1860 Government of India
  • Empanelled under Ministry of Horticulture and Food Processing, Government of Uttar Pradesh
  • Affiliated with Life Sciences and Food Industry Sector Skills Council (SSC) set up by National Skill Development Corporation (NSDC)
  • Conferred with QUALITY COUNCIL OF INDIA (QCI) – D.L. SHAH NATIONAL QUALITY AWARD & ASSOCHAM Services Excellence Award 2017

Trusted by organizations & training participants in over 30 countries
Training | Certification | Education | Research

Regulatory Affairs Programmes  Approved and Certified by Quality Council of India (QCI), Government of India

IGMPIs another addition to the hat of E/distance courses is comprehensive, interactive and intelligently structured Post Graduate and Executive Diploma course in Regulatory Affairs; targeting demand and supply disproportion of the healthcare industry. 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) has set laws and regulations when it comes to drugs 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, Bio technology laboratory or manufacturing unit or any other organization or unit of the healthcare industry, 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 e-course. The e-sessions, virtual classes, lectures, study material, self-assessment modules and certification exams all tend to motivate and make ready regulatory affair professionals with expertise in the field, to better serve the industry.

These e/distance courses have following tempting features which are definite to benefit one to all participants of the course:

• Comprehensive information, clearly targeting the healthcare industry;

• Well-structured course, intelligently put together under guidance of industry experts from same field;

• Easy to use, browse and explore e-tools woven remarkably well into the course make the study material, lectures, online database, examination preparation modules as well as assessment papers easily accessible.

• E-tools make the course self-paced and online exams make things easier and less complicated for the participants.

Post Graduate Diploma in Pharmaceutical Regulatory Affairs

Executive Diploma in Pharmaceutical Regulatory Affairs

For Food Industry Programmes, visit : (
For Healthcare Industry Programmes, visit: (
For Clinical Research Industry programmes, visit (
For Medical Coding Programmes, visit: (