의약품 관련 법령
Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Core Guideline Guidance for Industry
| 작성자 | 관리자 | ||
|---|---|---|---|
| 작성일 | 2018-07-31 | 조회수 | 752 |
| 국가정보 | 북 아메리카>미국 | ||
| 출처 | FDA | ||
| 원문 | https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM609205.pdf | ||
| 첨부파일 | |||
Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Core Guideline Guidance for Industry.pdf(450.61KB)Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Core Guideline Guidance for Industry
- 이전글 Q12 Technical and Regulatory Considerations for Pharmaceutical Product Lifecycle Management Annex
- 다음글 Waivers of the Single, Shared System REMS Requirement; Draft Guidance for Industry
