23 |
DETECTION OF RESIDUAL PENICILLINS IN DRUGS |
2003-02-25 |
22 |
Risk-Based Approach to 21 CFR Part 11 |
2003-02-24 |
21 |
Pharmaceutical cGMPs for the 21st Century |
2003-02-23 |
20 |
Pharmaceutical cGMP Initiative Questions and Answe |
2003-01-25 |
19 |
An Overview of the FDA’s PAT Initiative |
2003-01-23 |
18 |
How to Approach FDA Validation |
2003-01-22 |
17 |
KGMP 해설서- 정오표 |
2002-12-03 |
16 |
Guidance_Bioavailability_Bioequivalence |
2002-08-25 |
15 |
Development of Analytical Methods |
2002-08-24 |
14 |
Stability testing of biotechnological/biological p |
2002-08-23 |