의약품 관련 법령
Electronic product information for human medicines in the EU - draft key principles
작성자 | 관리자 | ||
---|---|---|---|
작성일 | 2019-01-31 | 조회수 | 1,190 |
국가정보 | 유럽>모든국가 | ||
출처 | EMA | ||
원문 | https://www.ema.europa.eu/en/electronic-product-information-human-medicines-european-union-draft-key-principles | ||
첨부파일 |
Electronic product information for human medicines in the EU - draft key principles
- 이전글 Draft guideline on quality, non-clinical and clinical requirements for investigational advanced therapy medicinal products in clinical trials
- 다음글 Draft ICH guideline M10 on bioanalytical method validation – step 2b