Centre for Pharmaceutical Sciences and Research (CPSAR)
(An Autonomous Body Recognized by Ministry of Commerce & Industry, Government of India)
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Analytical Testing and Equipment
Ayurvedic Cosmetology
Ayurvedic Formulations
Big-Data Analytics
Bioinformatics
Biomedical Technology
Biopharmaceutical Technology
Certificate in Pharmaceutical In Process Quality Assurance
Certificate in Quality Risk Management
Chemical Safety
Clinical SAS
Computer Aided Drug Design (CADD)
Computer Software Assurance
Computer System Validation
Computer System Validation
Cosmetic Technology
Data Integrity Professional
Dermacare Formulations
Digital Marketing
Documentation in QA & QC Department
Drug Discovery and Development
Drug Master File
Drug Registration (African)
Drug Registration (European Market)
Drug Registration (GCC)
Drug Registration (India)
Drug Registration (US-ANDA, NDA)
Drug Regulatory Affairs Professional
EU IVD Medical Device Regulation
European Union (EU) Medical Devices Regulation
Foundation Diploma in Life Sciences
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)
Good Laboratory Practices
Good Manufacturing Practices
Herbal Cosmetics
Herbal Drug Technology
Herbal Formulations
Herbal Formulations
HVAC Systems Validation
In Vitro Diagnostic Medical Device Directive ? CE Marking for Europe (98/79/EC)
Intellectual Property Rights
Lab Automation
Medical Device Management
Medical Device Professional (CMDP)
Medical Device Quality Auditor
Medical Device Regulatory Affairs Professional
Medical Devices Directive, CE Marking for Europe (93/42/EEC)
Medical Laboratory System (ISO 15189:2022) Internal Auditor
Medical Laboratory System (ISO 15189:2022) Lead Auditor
Medical Sales Representative
Nanomedicine
Nanotechnology
Pharmaceutical API Manufacturing
Pharmaceutical Automation
Pharmaceutical Business Analytics
Pharmaceutical Chemistry
Pharmaceutical Entrepreneurship
Pharmaceutical Formulation
Pharmaceutical GMP Auditor
Pharmaceutical GMP Professional
Pharmaceutical Management
Pharmaceutical Packaging
Pharmaceutical Process Engineering
Pharmaceutical Production
Pharmaceutical Quality Auditor
Pharmaceutical Quality Manager
Pharmaceutical Quality Technician
Pharmaceutical Regulatory Affairs
Pharmaceutical Sciences
Pharmaceutical Technology Transfer
Prescription to OTC Switch
Process Analytical Technology
Product Management
QA/QC (Medical Device as Major)
Quality Assurance and Quality Control
Quality by Design (QbD) Professional
Quality Management System for Medical Devices (ISO 13485)
Registration of Drug and Dossier Preparation (CTD and E CTD Submission)
Regulatory Affairs (Medical Device)
Regulatory Toxicology
Signal Detection and Data Mining
Stem Cell cGMP
Sterile Manufacturing
Technical Documentation (93/42/EEC)
Validation Professional
WHO-GMP Professional
Mode*
Online
Regular (Offline)
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