Institute of Good Manufacturing Practices India
(An Autonomous Body Recognized by Ministry of Commerce & Industry, Government of India)
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Analytical Testing and Equipment (PCATE)
Ayurvedic Formulations (PGDAF/EDAF)
Beauty Therapy & Makeup
Bioinformatics (PGDBI/EDBI)
Biological Product Registration (PCBPR)
Biomedical Technology (PGDBT/EDBT)
Biopharmaceutical Technology (PGGDBT/EDBT)
Certified Data Integrity Professional (CDIP)
Certified Drug Regulatory Affairs Professional (CDRAP)
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 Good Laboratory Practice Professional (CGLPP)
Certified Medical Device Professional (CMDP)
Certified Medical Device Quality Auditor (CMDQA)
Certified Medical Device Regulatory Affairs Professional (CMDRAP)
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 (CQRM)
Certified WHO-GMP Professional (PCWHO-GMP)
Chemical Technology (PGDCT/EDCT)
clinical cosmetology
Computer Aided Drug Design (PGDCADD/EDCADD)
Computer Software Assurance (PCCSA)
Computer System Validation (PCCSV)
Computer System Validation (PGDCSV/EDCSV)
Cosmetic Formulation Basics (CCFB)
Cosmetic Technology (PGDCT/EDCT)
Data Analytics (PGDDA/EDDA)
Dermacare Formulations (PGDDF/EDDF)
Digital Marketing
Documentation in QA & QC Department (PCDQAQCD)
Drug Discovery and Development (PGDDDD/EDDDD)
Drug Registration (African Countries) (PCDRAC)
Drug Registration (European Market) (PCDREM)
Drug Registration (GCC Countries) (PCDRGCCC)
Drug Registration (India) (PCDRI)
Drug Registration (US-ANDA, NDA)
Entrepreneurship in Cosmetic Science (CECS)
EU IVD Medical Device Regulation (PCEUIVDMDR)
European Union (EU) Medical Devices Regulation (PCEUMDR)
Foundation Diploma in Life Sciences
GMP (Indian Perspective)
GMP (International Perspective)
GMP (ROW Market)
GMP for Finished Pharmaceutical & for Manufacturing, Processing, Packing, or Holding of Drugs (PCGMPFPMPPHD)
Herbal Cosmetics (PGDHC/EDHC)
Herbal Drug Technology (PGDHDT/EDHDT)
Herbal Formulations (PCHF)
Herbal Formulations (PGDHF/EDHF)
HVAC Systems Validation (PCHVACSV)
In Vitro Diagnostic Medical Device Directive ? CE Marking for Europe (98/79/EC) (PCVDMDD)
Intellectual Property Rights (PGDIPR/EDIPR)
Lab Automation (PCLA)
Medical Device Management (PGDMDM/EDMDM)
Medical Devices Directive, CE Marking for Europe (93/42/EEC) (PCMDD)
Medical Sales Representative Training (PCMSRT)
Nanotechnology (PGDNT/EDNT)
Pharmaceutical API Manufacturing (PGDPAPIM/EDPAPIM)
Pharmaceutical Automation (PGDPA/EDPA)
Pharmaceutical Business Analytics (PGDPBA/EDPBA)
Pharmaceutical Business Management (PGDPBM/EDPBM)
Pharmaceutical Chemistry (PGDPC/EDPC)
Pharmaceutical Entrepreneurship (PCPE)
Pharmaceutical Formulation (PGDPF/EDPF)
Pharmaceutical Good Laboratory Practice (PGDGLP/EDGLP)
Pharmaceutical Good Manufacturing Practices (PGDGMP/EDGMP)
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)
Pharmaceutical Validation (PCPV)
Pharmacoinformatics (PGDPI/EDPI)
Preparation and Submission of Drug Master File (PCSDMF)
Prescription to OTC Switch (PCPOTCS)
Process Analytical Technology (PCPAT)
Professional Certification in Pharmaceutical In Process Quality Assurance (PCPPQA)
QA/QC (Medical Device as Major) (PGDQAMD/EDQAMD)
Quality Management System for Medical Devices (ISO 13485) (PCQMSMD)
Registration of Drug and Dossier Preparation (CTD and E CTD Submission)
Regulatory Affairs (Medical Device as Major) (PGDRAMDM/EDRAMDM)
Regulatory Toxicology (PGDRT/EDRT)
Stem Cell cGMP
Sterile Pharmaceuticals Manufacturing (PCSPM)
Technical Documentation (93/42/EEC)
WHO-GMP
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