Faculty of Pharmaceutical Sciences
(An Autonomous Body Recognized by Ministry of Commerce & Industry, Government of India)
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Analytical Testing and Equipment
Ayurvedic Formulations
Beauty Therapy & Makeup
Bioinformatics
Biological Product Registration (CBPR)
Biomedical Technology
Biopharmaceutical Technology
Certified Data Integrity Professional
Certified Drug Regulatory Affairs Professional
Certified GMP for AYUSH Professional
Certified GMP for Biological Products Professional
Certified GMP for Blood and Blood Components Professional
Certified GMP for Combination Products Professional
Certified GMP for Cosmetics Professional
Certified GMP for Herbal Medicines Professional
Certified GMP for Medical Devices Professional
Certified Good Laboratory Practice Professional (CGLPP)
Certified Medical Device Professional (CMDP)
Certified Medical Device Quality Auditor
Certified Medical Device Regulatory Affairs Professional
Certified Pharmaceutical GMP Auditor
Certified Pharmaceutical GMP Professional
Certified Pharmaceutical Quality Auditor
Certified Pharmaceutical Quality Manager
Certified Pharmaceutical Quality Technician
Certified Quality by Design (QbD) Professional
Certified Quality Risk Management
Certified WHO-GMP Professional
Chemical Technology
Clinical SAS
Computer Aided Drug Design (CADD)
Computer Software Assurance
Computer System Validation
Computer System Validation
Cosmetic Technology
Data Analytics
Dermacare Formulations
Digital Marketing
Documentation in QA & QC Department
Drug Discovery and Development
Drug Registration (African)
Drug Registration (European Market)
Drug Registration (GCC)
Drug Registration (India)
Drug Registration (US-ANDA, NDA)
EU IVD Medical Device Regulation
European Union (EU) Medical Devices Regulation
Foundation Diploma in Life Sciences
GMP for Finished Pharmaceutical & for Manufacturing, Processing, Packing, or Holding of Drugs
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 Devices Directive, CE Marking for Europe (93/42/EEC)
Medical Sales Representative
Nanotechnology
Pharmaceutical API Manufacturing
Pharmaceutical Automation
Pharmaceutical Business Analytics
Pharmaceutical Business Management
Pharmaceutical Chemistry
Pharmaceutical Entrepreneurship
Pharmaceutical Formulation
Pharmaceutical Good Laboratory Practice
Pharmaceutical Good Manufacturing Practices
Pharmaceutical Packaging
Pharmaceutical Process Engineering
Pharmaceutical Product Management
Pharmaceutical Production
Pharmaceutical Quality Assurance and Quality Control
Pharmaceutical Regulatory Affairs
Pharmaceutical Sciences
Pharmaceutical Technology Transfer
Preparation and Submission of Drug Master File (DMF)
Prescription to OTC Switch
Process Analytical Technology
Professional Certification in Pharmaceutical In Process Quality Assurance
QA/QC (Medical Device as Major)
Quality Management System for Medical Devices (ISO 13485)
Registration of Drug and Dossier Preparation (CTD and E CTD Submission)
Regulatory Affairs (Medical Device as Major)
Regulatory Toxicology
Signal Detection and Data Mining
Stem Cell cGMP
Sterile Manufacturing
Technical Documentation (93/42/EEC)
Validation Professional
Mode*
Online
Regular
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