E6(R2) good clinical practice: integrated addendum to ICH E6(R1)
- 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, March 2018
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Clinical Trials as Topic -- ethics Clinical Trials as Topic -- methods Ethics Committees, Research Informed Consent Randomized Controlled Trials as Topic -- ethics Randomized Controlled Trials as Topic -- methods Research Design Research Subjects Humans Europe Japan United States United States. Department of Health and Human Services. United States. Food and Drug Administration.
- Genre(s):
- Guideline 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 (iv, 63 pages)).
- NLM Unique ID:
- 101734075 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101734075