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Good Manufacturing Practices complementary to Experimental Drugs(ANVISA- BRAZIL)
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2020-01-20 | 조회수 | 622 |
| 원문 | |||
| 출처 | 한국보건산업진흥원 | ||
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| 첨부파일 | |||
Good Manufacturing Practices Complementary to Experimental Drugs.pdf (120 KB) -원문제목 : Guide for Good Manufacturing Practices complementary to Experimental Drugs, according to ANVISA- BRAZIL
-Abstract : This Normative Instruction is intended to adopt the Good Practice Guidelines for the Manufacturing of Experimental Drugs from the Pharmaceutical Inspection Cooperation Scheme, PIC/S, as complementary requirements to be followed in the manufacture of experimental drugs in addition to the General Good Practice Guidelines for Drug Manufacturing.
* 첨부파일 참고 바랍니다.
- 이전글 Good Practices on Drug Distribution, Storage and Transportation(ANVISA- BRAZIL)
- 다음글 Guide for the registration of active pharmaceutical ingredients (API), according to ANVISA- BRAZIL
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