의약품 관련 법령
Obligations concerning the reporting of post-authorisation adverse drug reactions in Hungary
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2020-02-20 | 조회수 | 760 |
| 국가정보 | 유럽>헝가리 | ||
| 출처 | |||
| 원문 | https://www.ogyei.gov.hu/Reporting%20requirements%20/ | ||
| 첨부파일 | |||
2019.8- Obligations concerning the reporting of post-authorisation adverse drug reactions in Hungary.pdf(126.69KB)Obligations concerning the reporting of post-authorisation adverse drug reactions in Hungary
- 이전글 Medicines for human use and others, amending the laws governing the pharmaceutical market
- 다음글 The pre-ion and dispensing of medicinal products for human use
