| 92 |
Cleaning Validation in API Plants_2000 |
2008-04-08 |
| 91 |
FDA CDER Guidance Agenda |
2008-03-13 |
| 90 |
Container and Closure System Integrity Testing in Lieu of Sterility Testing |
2008-03-03 |
| 89 |
EU GMP Annex 20 Quality Risk Management |
2008-02-21 |
| 88 |
EU GMP Chapter 1. Quality Management |
2008-02-21 |
| 87 |
EU GMP Annex 1. 신구 대비 |
2008-02-21 |
| 86 |
EU GMP Annex 1. Manufacture of sterile medicinal products |
2008-02-21 |
| 85 |
FDA 약어집 |
2008-02-18 |
| 84 |
FDA CDER List of Guidance Document |
2008-02-04 |
| 83 |
의약품등 밸리데이션 실시에 관한 규정 고시 원문 |
2008-01-18 |
