Institute of Good Manufacturing Practices India
Global accredited training provider
Approved by Quality Council of India (QCI), Government of India
An ISO 9001:2008 Certified Organisation
Registered under the society Registration Act, 1860, Government of India
Permanently Empanelled under ministry of Horticulture and Food Processing, Government of Uttar Pradesh
Recipient of QCI – D.L. Shah National Quality Award – Certificate of Merit 2015
New Delhi | Noida | Hyderabad | Lucknow

Trusted by training participants in over 20 countries


This course provides an overview of PAT applications in pharmaceutical operations. At the end of the course, participants will get to know the PAT life cycle, PAT applications likely to yield positive benefit, understand issues of organizing and managing a PAT project and integrating the principles of Quality by Design into the effort. Process analytical technology (PAT) is becoming a very important tool for controlling pharmaceutical processes and when implementing Quality by Design. This course is designed to help pharmaceutical manufacturing professionals chart a new course for innovation based on PAT.

Module 1 :PAT Vision and Framework

Module 2 :PAT in Development, Manufacturing, Automation control system, Quality by design, Process validation etc.


Any Life Science graduate/ B.Pharm/M pharm/MSc/Phd in science disciplines/ any diploma holder or passed outs of Clinical Research degree or diploma courses are eligible for these course. Working professionals of any of the following industry types Drugs manufacturing , Medical Device, Ayurveda, Pharmaceutical Industry Regulation, Clinical Research, Homeopathic or Ayurveda Medicine Manufacturing, Cosmetic Manufacturing, Biotechnology or any related industry are highly encouraged to apply for the programme.

Programme Duration

The candidate is expected to complete the course in a minimum of 1 and maximum of 3 months.


The registration dates for this programme run by the institute are updated timely on the webpage. Effective E-learning tools incorporated into the design of the webpage make the course lectures, videos and study material easily accessible. This gives huge window of self regulated and self-paced performance to the participants.

Programmes Fees

A one-time fees (lump sum paid at beginning of the course) of Rs 7,500/- (300 USD for oversees students) is mandatory. This covers for the course registration fees, tuition fees, course material examination fee etc.

Examination & Certification

All the participants are expected to appear for online exam and are also obliged to submit assignments after each module. After successful completion the participants will be awarded Certificate in Process Analytical Technology by IGMPI. For all the above mentioned modules elaborate course material, assignment and case studies would be provided by the Institute from time to time. Details get updated on the webpage as well.

Corporate Relations

In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy's Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, IPCA Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy , Biocon etc. The IGMPI's Corporate Resource Division actively recommends our students and training participants for various job requirements and specialized roles to Human Resource, Talent Acquisition as well as the heads of various departments in Pharmaceutical, Healthcare and Food industries on regular basis.

Future career prospects

Process Analytical Technology is becoming a very important tool for controlling pharmaceutical processes and when implementing quality by design. This course provides an overview to the tools and principles outlined in the FDA guidance. This course is very useful for professional engineers, scientists and managers involved in pharmaceutical drug substance or drug product manufacturing and development, quality assurance and regulatory affairs.

For further enquiries or Prospectus, write to or call us on:

[email protected]/+91 8130924488



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