의약품 관련 법령
PEI Information Note: Requirements in Accordance with the Falsified Medicines Directive (Directive 2011/62/EC)
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2018-12-07 | 조회수 | 1,208 |
| 국가정보 | 유럽>독일 | ||
| 출처 | PEI | ||
| 원문 | www.pei.de | ||
| 첨부파일 | |||
PEI Information Note_ Requirements in Accordance with the Falsified Medicines Directive (Directive 2011_62_EC).pdf(212.61KB)
This document informs on the implementations of regulatory requirements in Accordance with the Falsified Medicines Directive (Directive 2011/62/EC) for:
- Medicinal products authorized under European procedures;
- Nationally approved medicinal products.
In the update of Oct-2018, the document was revised and the links to the document "European Parliament and Council Directive 2011/62/EU of 08-Jun-201...
- Medicinal products authorized under European procedures;
- Nationally approved medicinal products.
In the update of Oct-2018, the document was revised and the links to the document "European Parliament and Council Directive 2011/62/EU of 08-Jun-201...
- 이전글 BfArM: Information Note on the Electronic Declaration of Marketed Medicinal Products Not Requiring Marketing Authorization
- 다음글 BfArM Information Note: Requirements According to the Falsified Medicines Directive (Directive 2011/62/EC)
