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 | 1,398 |
| 국가정보 | 북 아메리카>미국 | ||
| 출처 | FDA | ||
| 원문 | https://www.fda.gov/ucm/groups/fdagov-public/@fdagov-drugs-gen/documents/document/ucm333969.pdf | ||
| 첨부파일 | |||
ucm333969.pdf(121.22KB)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
