의약품 관련 법령
Providing Regulatory Submissions in Electronic Format - Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications
작성자 | 관리자 | ||
---|---|---|---|
작성일 | 2019-01-29 | 조회수 | 1,425 |
국가정보 | 북 아메리카>미국 | ||
출처 | FDA | ||
원문 | https://www.fda.gov/ucm/groups/fdagov-public/@fdagov-drugs-gen/documents/document/ucm333969.pdf | ||
첨부파일 |
Providing Regulatory Submissions in Electronic Format - Certain Human Pharmaceutical Product Applications and Related Submissions Using the eCTD Specifications
- 이전글 Labeling for Human Pre-ion Drug and Biological Products Approved Under the Accelerated Approval Regulatory Pathway
- 다음글 Providing Lot Release Protocol Submissions to the Center for Biologics Evaluation and Research(CBER) in Electronic Format