01
Session 1
Overview of Quality Control in GMP
02
Session 2
Good Quality Control Laboratory Practices
03
Session 3
Laboratory Design Audit
04
Session 4
Documentation and Data Integrity in QC
05
Session 5
Sampling Techniques and Best Practices
06
Session 6
Testing and Validation in QC
07
Session 7
Analytical Methods Development
08
Session 8
Method validation
09
Session 9
Method Transfer
10
Session 10
Managing OOS/OOT Results
11
Session 11
Stability Studies and Shelf-Life Evaluation
12
Session 12
Technical Transfer of Testing Methods
13
Session 13
QC in a GMP Environment: Challenges and Best Practices
14
Session 14
QC testing learning platforms
Our Courses
- Introduction to GMDP Regulations and Importance of GMDP
- Pharmaceutical Quality System (PQS)
- Personnel
- Premises and Equipments
- Documentation
- Production
- Quality Control
- Outsource Activities
- Complaints, Quality Defects, and Product Recalls
- Self-Inspection and Audit
- Good Distribution Practice (cGDP)
- Regulatory Affairs & Regulatory Submissions