Institute of Good Manufacturing Practices India

Competency based training & PG Diploma programmes

Excellent Placement Record

Admission Notice

Admissions Enquiry & Counselling:
18001031071 (Toll Free), Phone: +91 11 26512850 (9:00 am to 5:30 pm IST-except on Central Government holidays)/ info@igmpi.ac.in

Last date for submitting completed Application Form: 18^th May 2026 (Session April-May, 2026). Do not wait for last date to avoid server issues.

Modes available:

Part-time (Online Live Classes)
Regular Mode

Fill up to receive Prospectus & admission details

CAPTCHA:

Cosmetic Technology (PGDCT/EDCT)

Pharmaceutical Quality Assurance and Quality Control (PGDPQAQC/EDPQAQC)

Good Manufacturing Practices (PGDGMP/EDGMP)

Herbal Cosmetics (PGDHC/EDHC)

Dermacare Formulations (PGDDF/EDDF)

Ayurvedic Formulations (PGDAF/EDAF)

Pharmaceutical Regulatory Affairs (PGDPRA/EDPRA)

Pharmaceutical Production (PGDPP/EDPP)

Pharmaceutical API Manufacturing (PGDPAM/EDPAM)

Pharmaceutical Formulation (PGDPF/EDPF)

Pharmaceutical Process Engineering (PGDPPE/EDPPE)

Pharmaceutical Packaging (PGDPP/EDPP)

Pharmaceutical Technology Transfer (PGDPTT/EDPTT)

Pharmaceutical Chemistry (PGDPC/EDPC)

Pharmaceutical Sciences (PGDPS/EDPS)

Regulatory Toxicology (PGDRT/EDRT)

Pharmaceutical Good Laboratory Practice (PGDPGLP/EDPGLP)

Pharmacoinformatics (PGDPI/EDPI)

Big Data Analytics (PGDDA/EDDA)

Pharmaceutical Business Analytics (PGDPBA/EDPBA)

Biopharmaceutical Technology (PGDBT/EDBT)

Drug Discovery and Development (PGDDDD/EDDDD)

Computer Aided Drug Design (PGDCADD/EDCADD)

Bioinformatics (PGDBI/EDBI)

Intellectual Property Rights (PGDIPR/EDIPR)

Pharmaceutical Product Management (PGDPPM/EDPPM)

Pharmaceutical Business Management (PGDPBM/EDPBM)

Herbal Drug Technology (PGDHDT/EDHDT)

Chemical Technology (PGDCT/EDCT)

Computer System Validation (PGDCSV/EDCSV)

Data Analytics (PGDDA/EDDA)

Foundation Diploma in Life Sciences (FDLS)

Herbal Formulations (PGDHF/EDHF)

Medical Device Management (PGDMDM/EDMDM)

Nanotechnology (PGDNT/EDNT)

Pharma Diploma Programmes

Pharmaceutical Automation (PGDPA/EDPA)

Quality Assurance and Quality Control (Medical Device as major) (PGDQAMD/EDQAMD)

Regulatory Affairs (Medical Device as Major) (PGDRAMDM/EDRAMDM)

Computer System Validation (PCCSV)

Herbal Formulations (PCHF)

Analytical Testing and Equipment (PCATE)

Biological Product Registration (PCBPR)

Certified Data Integrity Professional (CDIP)

Certified Drug Regulatory Affairs Professional (CDRA)

Certified GMP for AYUSH Professional (CGMPA)

Certified GMP for Biological Products Professional (CGMPBPP)

Certified GMP for Blood and Blood Components Professional (CGMPBBCP)

Certified GMP for Combination Products Professional (CGMPCPP)

Certified GMP for Cosmetics Professional (CGMPC)

Certified GMP for Herbal Medicines Professional (CGMPHM)

Certified GMP for Medical Devices Professional (CGMPMD)

Certified Medical Device Professional (CMDP)

Certified Medical Device Quality Auditor (CMDQA)

Certified Medical Device Regulatory Affairs (CMDRA)

Certified Pharmaceutical GMP Auditor (CPGMPA)

Certified Pharmaceutical GMP Professional (CPGMP)

Certified Pharmaceutical Quality Auditor (CPQA)

Certified Pharmaceutical Quality Manager (CPQM)

Certified Pharmaceutical Quality Technician (CPQT)

Certified Quality by Design (QbD) Professional (CQBD)

Certified Quality Risk Management Professional (CQRM)

Certified WHO - GMP Professional (PCWHO-GMP)

Computer Software Assurance (PCCSA)

Documentation in QA & QC Department (PCDQAQCD)

Drug Registration (African countries) (PCDRAC)

Drug Registration (European market) (PCDREM)

Drug Registration (GCC countries) (PCDRGCCC)

Drug Registration (India) (PCDRI)

Drug Registration (US Market-ANDA, NDA etc)

EU IVD Medical Device Regulation (PCEUIVDMDR)

EU Medical Devices Regulation (PCEUMDR)

GMP for Finished Pharmaceutical & for Manufacturing, Processing, Packing, or Holding of Drugs (PCGMPFPMPPHD)

Good Laboratory practice professional (CGLPP)

HVAC Systems Validation (PCHVACSV)

In Vitro Diagnostic Medical Device Directive – CE Marking for Europe (98/79/EC) (PCVDMDD)

Lab Automation (PCLA)

Medical Devices Directive, CE Marking for Europe (93/42/EEC) (PCMDD)

Medical Sales Representative Training (PCMSRT)

Pharmaceutical Entrepreneurship (PCPE)

Pharmaceutical In Process Quality Assurance (PCPPQA)

Pharmaceutical Microbiology (PCPM)

Pharmaceutical Validation (PCPV)

Preparation and Submission of Drug Master File (PCSDMF)

Prescription to OTC Switch (PCPOTCS)

Process Analytical Technology (PCPAT)

Registration of Drug and Dossier Preparation (CTD and eCTD submissions)

Stem Cell cGMP

Sterile Pharmaceuticals Manufacturing (PCSPM)

Technical Documentation (93/42/EEC)

Cosmetic Formulation & Lab Practices

Cosmetic Formulation Basics (CCFB)

GMP (Indian Perspective)

GMP (International Perspective)

GMP (ROW Market)

ISO 14971:2019 Risk Management for Medical Devices

WHO-GMP

Short-Term Programmes

Certificate Programmes

Entrepreneurship in Cosmetic Science (CECS)

Clinical Psychology Programmes

Faculty of AYUSH Programmes

Medical Coding Programmes

Post Graduate Diploma / Executive Diploma (PGD/ED)

Clinical Psychology (PGCP/EDCP)

Digital Forensics (PGDF/EDF)

Forensic Science (PGFS/EFS)

Medical Coding (PGDMC/EDMC)

Public Health and Hospital Management (PGDPHHM/EDPHHM)

Food Science and Technology (PFGFST/EFST)

Clinical Research (PGCR/ECR)

Environment Health and Safety (PGDEHS/EDEHS)

Pharmacovigilance (PGPV/EPV)

Environmental Law and Policy (PGDELP/EDELP)

Environmental Studies and Resources Management (PGDESRM/EDESRM)

Forensic Accounting and Fraud Investigation (PGFAFI/EDFAFI)

Forensic Regulatory Affairs (PGFRA/EFRA)

Professional Certification

Environmental Social and Governance (PCESG)

Clinical SAS (PCSAS)

Drug Safety Aggregate Reporting (DSAR)

SCADA Lead Security Manager

Signal Detection and Data Mining (SDDM)

Trial Master File (TMF) Management (TMF)

Medical Laboratory System (ISO 15189:2022) Internal Auditor (MLSIA) (3 days)

Medical Laboratory System (ISO 15189:2022) Lead Auditor (MLSLA) (5 days)

About Us

The Institute of Good Manufacturing Practices India, an autonomous Institute 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, Nutrition 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, Environment 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.

IGMPI a part of the Grand Jury for the prestigious Nutriwell Conclave and Healthcare Awards, 2025: Our Director presenting the awards nutrition-wellness-award-2025