| 620 |
첫 제약바이오 RA전문 교과서 출판되다~! |
2023-04-08 |
| 619 |
EQPA Code of Practice for QPs - Duties and Responsibilities for Qualified Persons in the EU |
2023-03-06 |
| 618 |
ICH Q9 (R1) Quality Risk Management 확정 발표 |
2023-02-15 |
| 617 |
EU GMP Annex 1개정판(2022)과 이전 버전 비교 |
2023-02-08 |
| 616 |
FDA Gudiance for Industry: M10 Bioanalytical Method Validation and Study Sample Analysis |
2023-01-27 |
| 615 |
ICH Q13 Continuous Manufacturing of Drug Substances and Drug Products 발표 |
2023-01-17 |
| 614 |
FDA Guidance for Industry(draft): Delaying, Denying, Limiting, or Refusing Inspection |
2023-01-13 |
| 613 |
Contamination Control Strategy Guideline |
2022-12-21 |
| 612 |
IPEC-PQG GMP for Excipients |
2022-12-17 |
| 611 |
OECD의 GLP분야 Data Integrity Guidelines |
2022-11-19 |
