Pharmaceutical Industries Guidelines
- Quality Control – Principle, General information – EU GMP
- Microbiological Control Tests
- Daily Maintenance and Common problems in HPLC
- Infrared Absorption Spectroscopy
- HPLC Basics- Principle and Scope
- Aseptic Processing – Sterile Pharmaceutical
- Good Laboratory Practice – GLP
- Out of Specification (OOS)
- SCHEDULE M – GMP – PART 1
- SCHEDULE M – GMP – PART 2 (OSD)
- SCHEDULE M – GMP – PART 3 (PARENTERAL PREPARATIONS)
- SCHEDULE M – GMP – PART 4 (ORAL LIQUIDS)
- SCHEDULE M – GMP – PART 5 (TOPICAL PRODUCTS)
- SCHEDULE M – GMP – PART 6 (METERED-DOSE-INHALERS)
- SCHEDULE M – GMP – PART 7 (API-BULK DRUGS)
- SCHEDUE M-I
- SCHEDULE M-II
- Dissolution Test
- Loss on drying
- Residue on ignition / Sulfated ash
- Karl Fischer Titration
- Disintegration Test
- SCHEDULE L-1 (GLP)
- ICH Guidelines
- Bursting Strength Tester
- What is CAPA – Corrective and preventative action
- Data Integrity – ALCOA+
- Limit Tests
- Pharmaceutical Quality System – EU GMP
- Personnel – EU GMP
- Premises and Equipment – EU GMP
- Documentation – EU GMP
- Production – EU GMP
- Outsourced Activities – EU GMP
- Complaints and Product Recalls – EU GMP
- Self Inspection – EU GMP
- Site Master File – EU GMP
- Containers-Glass
- 21 CFR Part 211-cGMP