Adaptive designs for clinical trials of drugs and biologics
- Collection:
- Health Policy and Services Research
- Series Title(s):
- Guidance for industry
- Contributor(s):
- United States. Department of Health and Human Services, issuing body. United States. Food and Drug Administration, issuing body. Center for Biologics Evaluation and Research (U.S.), issuing body. Center for Drug Evaluation and Research (U.S.), issuing body.
- Publication:
- Silver Spring, MD : Center for Drug Evaluation and Research, November 2019
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Adaptive Clinical Trials as Topic -- standards Investigational New Drug Application Adaptive Clinical Trials as Topic -- ethics Biological Products Drugs, Investigational Research Design Humans United States United States. Department of Health and Human Services. United States. Food and Drug Administration.
- Genre(s):
- Technical Report
- Copyright:
- The National Library of Medicine believes this item to be in the public domain. (More information)
- Extent:
- 1 online resource (1 PDF file (33 pages)).
- NLM Unique ID:
- 101760568 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101760568