Centre for Pharmaceutical Sciences and Research (CPSAR)
Centre for Pharmaceutical Sciences and Research (CPSAR)

(An Autonomous Body Recognized by Ministry of Commerce & Industry, Government of India)

Regular Classroom | Online Mode
Job Competency based Post Graduate Diploma's and Professional Certifications
Excellent Placement Record
Admission Notice
Admissions are open now.

Admissions Enquiry & Counselling:
18001031071 (Toll Free -9:00 am to 5:30 pm IST-except on Central Government holidays)/ info@igmpi.ac.in

WhatsApp

Last date for submitting completed Application Form is 6th May 2025. (Limited seats only)

Fill up this form to receive the Prospectus along with full admissions details
Post Graduate Diploma / Executive Diploma (PGD/ED)
Ayurvedic Cosmetology (PGDAC/EDAC)
Ayurvedic Formulations (PGDAF/EDAF)
Big Data Analytics (PGDBDA/EDBDA)
Bioinformatics (PGDBI/EDBI)
Biopharmaceutical Technology (PGDBT/EDBT)
Computer Aided Drug Design (PGDCADD/EDCADD)
Computer System Validation (PGDCSV/EDCSV)
Cosmetic Technology (PGDCT/EDCT)
Dermacare Formulations (PGDDF/EDDF)
Digital Marketing (PGDDM/EDDM)
Drug Discovery and Development (PGDDDD/EDDDD)
Good Manufacturing Practices (PGDGMP/EDGMP)
Herbal Cosmetics (PGDHC/EDHC)
Herbal Drug Technology (PGDHDT/EDHDT)
Herbal Formulations (PGDHF/EDHF)
Herbal Medicine (PGDHM/EDHM)
Intellectual Property Rights (PGDIPR/EDIPR)
Medical Device Management (PGDMDM/EDMDM)
Nanotechnology (PGDNT/EDNT)
Pharma Diploma Programmes
Pharmaceutical API Manufacturing (PGDPAM/EDPAM)
Pharmaceutical Automation (PGDPA/EDPA)
Pharmaceutical Business Analytics (PGDPBA/EDPBA)
Pharmaceutical Business Management (PGDPBM/EDPBM)
Pharmaceutical Chemistry (PGDPC/EDPC)
Pharmaceutical Formulation (PGDPF/EDPF)
Pharmaceutical Good Laboratory Practice (PGDPGLP/EDPGLP)
Pharmaceutical Packaging (PGDPP/EDPP)
Pharmaceutical Process Engineering (PGDPPE/EDPPE)
Pharmaceutical Product Management (PGDPPM/EDPPM)
Pharmaceutical Production (PGDPP/EDPP)
Pharmaceutical Quality Assurance and Quality Control (PGDPQAQC/EDPQAQC)
Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA)
Pharmaceutical Sciences (PGDPS/EDPS)
Pharmaceutical Technology Transfer (PGDPTT/EDPTT)
Quality Assurance and Quality Control (Medical Device as major) (PGDQAMD/EDQAMD)
Regulatory Affairs (Medical Device as Major) (PGDRAMDM/EDRAMDM)
Regulatory Toxicology (PGDRT/EDRT)
Biomedical Technology (PGDBT/EDBT)
Certificate Programmes
Analytical Testing and Equipment
Biological Product Registration (CBPR)
Chemical Safety
Clinical SAS
Computer Software Assurance
Computer System Validation (CCSV)
Documentation in QA & QC Department
Drug Registration (African countries)
Drug Registration (European market)
Drug Registration (GCC countries)
Drug Registration (India)
Drug Registration (US Market-ANDA, NDA etc)
Drug Safety Aggregate Reporting
EU IVD Medical Device Regulation
EU Medical Devices Regulation
Foundation Diploma in Life Sciences (FDLS)
GMP for Finished Pharmaceutical & for Manufacturing, Processing, Packing, or Holding of Drugs
Herbal Formulations
HVAC Systems Validation
In Vitro Diagnostic Medical Device Directive – CE Marking for Europe (98/79/EC)
Lab Automation
Medical Devices Directive, CE Marking for Europe (93/42/EEC)
Medical Sales Representative
Nanomedicine
Pharmaceutical Entrepreneurship
Pharmaceutical In Process Quality Assurance (IPQA)
Preparation and Submission of Drug Master File (DMF)
Prescription to OTC Switch
Process Analytical Technology
Registration of Drug and Dossier Preparation (CTD and eCTD submissions)
Signal Detection and Data Mining
Stem Cell cGMP
Sterile Manufacturing
Technical Documentation (93/42/EEC)
Technical Documentation (93/42/EEC)
Quality Management System for Medical Devices (ISO 13485)
Professional Certification
Data Integrity Professional
Drug Regulatory Affairs Professional
GMP for AYUSH Professional
GMP for Biological Products Professional
GMP for Blood and Blood Components Professional
GMP for Combination Products Professional
GMP for Cosmetics Professional
GMP for Herbal Medicines Professional
GMP for Medical Devices Professional
Good Laboratory practice professional(CGLPP)
Medical Device Professional (CMDP)
Medical Device Quality Auditor
Medical Device Regulatory Affairs Professional
Medical Laboratory System (ISO 15189:2022) Internal Auditor (3 days)
Medical Laboratory System (ISO 15189:2022) Lead Auditor (5 days)
Pharmaceutical GMP Auditor
Pharmaceutical GMP Professional
Pharmaceutical Quality Auditor
Pharmaceutical Quality Manager
Pharmaceutical Quality Technician
Professional Validation
Quality by Design (QbD) Professional
Quality Risk Management Professional
WHO - GMP Professional

Other Programmes

Post Graduate Diploma / Executive Diploma (PGD/ED)
Medical Coding (PGDMC/EDMC)
Clinical Psychology (PGDCP/EDCP)
Clinical Research (PGDCR/EDCR)
Environment Health and Safety (PGDEHS/EDEHS)
Environment Regulatory Affairs (PGDERA/EDERA)
Environmental Studies and Resources Management (PGDESRM/EDESRM)
Food Science and Technology (PGDFST/EDFST)
Nutrition and Dietetics (DND)
Pharmacovigilance (PGDPV/EDPV)
Public Health and Hospital Management (PGDPHHM/EDPHHM)

About

The Institute of Good Manufacturing Practices India, registered under SR Act XXI of 1860, Government of India, recognised by Ministry of Commerce & Industry, accredited Vocational Institution of Ministry of Education, Government of India and approved by Food Safety and Standards Authority of India (FSSAI) presents a unique, friendly and interactive platform to get rid of all your GMP compliance related issues. GMP- an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing and sustainability services - in itself is the most dynamic part which witnesses frequent changes in terms of new rules being added and old ones being renewed. Thus, keeping oneself updated with current GMPs is essential to remain aligned with evolving industry requirement and standards.

Our team comprises knowledgeable professionals from diverse sectors such as Pharma, Healthcare, Food & Nutraceutical industries, pooling together their expertise, know-how, and practical experiences to create this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as a stronger and better education and training platform provider for professionals and students in the areas of GMP, Quality Assurance and Control, Pharma, Food & Nutrition and Healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. Our board of governors and specialists have collated their acumen and are offering state-of-the-art courses which includes GMP training, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR, Environment Social Governance (ESG), and Good Laboratory Practice in form of formal classroom studies, online/interactive programmes, online seminars, as well as onsite training programmes along with the knowledge of worldwide affairs of the industry. In short, a round-the-clock service is provided for any information in these areas required by anybody from around the country and abroad. Based on high standards of quality, the training programmes in Pharma, Healthcare and Food GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management, Public Health, Hospital Management, Clinical Research, Pharmacovigilance, Medical Writing, Medical Coding, Nanotechnology, Drug Design and Discovery, Food QA&QC, etc., areas have been approved by Quality Council of India, which is an autonomous body and an accreditation authority for education & vocational training providers under the Ministry of Commerce & Industry, Government of India. IGMPI is duly licensed and certified by Bureau of Indian Standards (BIS) under Bureau of Indian Standards (Conformity Assessment) Regulations 2018.

Programmes Features

  • An autonomous Institute recognized by the Ministry of Commerce & Industry, Government of India
  • A nationally and internationally accredited Institute. The details available on our accreditation page.
  • IGMPI is certified and licensed by Bureau of Indian Standards (BIS)
  • Accredited Vocational Institution of Ministry of Education, Government of India
  • Approved Training Institute of Food Safety and Standards Authority of India (FSSAI)
  • IGMPI is an Institutional Member of the International Society for Quality in Healthcare (ISQua)
  • IGMPI Certifications demonstrate your professional accomplishment and proficiency leading towards professional credentialing
  • Industry endorsed programmes
  • Post Graduate Diploma is 12 months 'duration programme while Executive Diploma/Industry Diploma is an advanced and fast-track programme of 6 months' duration
  • A team of experts who are highly qualified, professionally competent and dedicated have been engaged as the faculty
  • Comprehensive, dynamic and advanced study material in an international perspective along with case study based approach
  • A fee concession of 10% is applicable to candidates belonging to SC/ST/Physically handicapped /Weaker Section(EWS)/Ex-servicemen for PG Diploma Courses
  • Classes, practicals and online demonstrations (as per weekly schedule) by highly qualified faculty and industry professionals; Regular students' support throughout the duration of the programme.
  • Accredited laboratory facility
  • Placement assistance by a robust and proactive placement cell under the supervision of the Director to kindle the flame of talent
  • Graduates and the candidates appearing for the final year of Bachelor's degree/equivalent qualification exam or awaiting their results are also eligible to apply.
Conferment of the prestigious "BUREAU OF INDIAN STANDARDS (BIS) AWARD OF HONOUR 2023" to IGMPI
IGMPI is Conferred with QCI - D. L. Shah Quality Award
ASSOCHAM Services Excellence Award 2017

Modes available:

  • Full Time Class Room Programmes
  • Online mode (Online Live Classes on Sundays on all the programme modules along with hard copies of Comprehensive study resources)
IGMPI PLACEMENT