의약품 관련 법령
ANMAT-MED CDF 001-00: Good manufacturing Practice Non-compliance Classification
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2018-12-04 | 조회수 | 998 |
| 국가정보 | 남 아메리카>아르헨티나 | ||
| 출처 | ANMAT | ||
| 원문 | http://opinion_publica.anmat.gov.ar | ||
| 첨부파일 | |||
Good manufacturing Practice Non-compliance Classification.pdf(820.98KB)
This document is a Draft of a tool to be used for the classification of the non-compliances detected in good manufacturing practice inspections in accordance with a risk-base quality assessment.
- 이전글 Disposition 2089/2018: Documents to be Used as Proof of Commercialization for the Grant of Marketing Authorization within Decree 150/92
- 다음글 Resolution RDC 20: Regulates About the Electronic Submission Procedure Applied to the Registration (Marketing Authorization) of New Medicinal Products
