의약품 관련 법령
Assessing User Fees Under the Pre-ion Drug User Fee Amendments of 2017 Guidance for Industry
작성자 | 관리자 | ||
---|---|---|---|
작성일 | 2018-07-31 | 조회수 | 1,187 |
국가정보 | 북 아메리카>미국 | ||
출처 | FDA | ||
원문 | https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM580099.pdf | ||
첨부파일 |
Assessing User Fees Under the Prescription Drug User Fee Amendments of 2017 Guidance for Industry
- 이전글 한국과 중국의 의약품 인허가 체계비교
- 다음글 Waivers, Exceptions, and Exemptions from the Requirements of Section 582 of the Federal Food, Drug, and Cosmetic Act Guidance for Industry