의약품 관련 법령
Guideline for Participants at the Joint Pilot Project of Competent Federal Authorities and Ethics Committees for Treatment of Clinical Trial Applications with Medicinal Products for Human Use According to Regulation (EU) No 536/2014 with Respect of Legal Provisions Set up in the German Drug Law and GCP-Decree
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2018-05-17 | 조회수 | 690 |
| 국가정보 | 유럽>독일 | ||
| 출처 | BfArM | ||
| 원문 | www.bfarm.de | ||
| 첨부파일 | |||
Guideline for Participants at the Joint Pilot Project of Competent Federal Authorities and Ethics Committees for Treatment.pdf(335.46KB)
Guideline for Participants at the Joint Pilot Project of Competent Federal Authorities and Ethics Committees for Treatment of Clinical Trial Applications with Medicinal Products for Human Use According to Regulation (EU) No 536/2014 with Respect of Legal Provisions Set up in the German Drug Law and GCP-Decree
- 이전글 DIMDI Announcement of 16-May-2018: On Amendments According to §5 of the Decree on Determination and Labeling of Pack Sizes for Medicinal Products
- 다음글 Regulation of the Federal Ministry of Health: Repeal of the Regulation on Test Measures for the Introduction of the Electronic Health Card
