Quality Control
Build expertise in analytical testing, instrumentation and pharmacopoeial standards.
Overview
This course trains students in pharmaceutical quality control practices including analytical method validation, instrumentation (HPLC, GC, UV-Vis, dissolution testing), pharmacopoeial standards (IP/BP/USP), stability testing and QC documentation. Graduates are prepared for laboratory-based QC roles in pharma manufacturing and testing laboratories.
Eligibility
- B.Pharm
- M.Pharm
- Pharm.D
- Life Sciences Graduates
- Freshers and working professionals
Course Duration
3 Months (Weekday & Weekend batches available)
Career Opportunities
- Quality Control Analyst
- QC Chemist
- Analytical Method Validation Associate
- Stability Study Coordinator
- QC Documentation Executive
Training Features
- Hands-on training on HPLC, GC and dissolution apparatus concepts
- Pharmacopoeial standards (IP/BP/USP) workshops
- Method validation and stability study exercises
- Experienced QC industry trainers
- Placement support with pharma testing labs
Enquire About Quality Control
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