| Mar 2025 | ||||||
|---|---|---|---|---|---|---|
| Mon | Tue | Wed | Thu | Fri | Sat | Sun |
| 01 | 02 | |||||
| 03 | 04 | 05 | 06 | 07 | 08 | 09 |
| 10 | 11 | 12 | 13 | 14 | 15 | 16 |
| 17 | 18 | 19 | 20 CMO Supplier Quality Agreements – How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture | 21 | 22 | 23 |
| 24 | 25 | 26 Sterile Filtration of Pharmaceutical Products – Validation and Regulatory Requirements | 27 Risk Management of Raw Materials in a GMP Environment | 28 | 29 | 30 |
| 31 | ||||||
| Prev Next | ||||||