| 624 |
의약품 GMP 적합판정 및 적합판정서 발급 관련 업무처리방안(공무원지침서) |
2023-10-09 |
| 623 |
Revision of the PIC/S and EU GMP Guides and Annexes |
2023-08-29 |
| 622 |
Annex 1. PUPSIT 의 득과 실 |
2023-07-15 |
| 621 |
PIC/S GMP Guide PE 009-17 (25 August 2023) 발표 |
2023-07-09 |
| 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 |
