An advanced 2-year (4-semester) postgraduate degree focused on system validation, quality control, regulatory compliance, and cGMP standards in pharmaceutical manufacturing and development.
4 Semesters
Regulatory Body
Affiliated
Quality Standards
The Master of Pharmacy (M.Pharm) in Quality Assurance is a 2-year (4-semester) postgraduate program that focuses on system validation, quality control, regulatory compliance, and cGMP standards required in pharmaceutical manufacturing and development.
The course trains postgraduates to implement global quality standards (ICH, US-FDA, WHO-GMP), perform advanced analytical testing, handle documentation, and manage process validation to ensure safety, efficacy, and batch-to-batch consistency.
Core modules and specialized competencies emphasized throughout the curriculum:
Quality Risk Management and cGMP compliance guidelines implementation.
Modern analytical method development and validation using HPLC, GC, and UV-Vis spectroscopy.
International regulatory affairs, dossier audits, and regulatory submissions.
Validation protocols for manufacturing equipment, processing facilities, and analytical procedures.
Candidates applying for admission to M.Pharm in Quality Assurance must fulfill the following criteria:
Admissions are processed through KEA PGCET central counseling seat allocation as well as Management Quota seats.
Graduates are highly sought after by domestic and international pharmaceutical companies for key compliance and executive roles: