Use of electronic health record data in clinical investigations
- 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 Devices and Radiological Health (U.S.), issuing body. Center for Drug Evaluation and Research (U.S.), issuing body.
- Publication:
- Silver Spring, MD : Center for Drug Evaluation and Research, July 2018
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Clinical Trials as Topic Electronic Health Records -- utilization Health Information Interoperability Forms and Records Control Informed Consent Reproducibility of Results Single-Blind Method Humans 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 (12 pages)).
- NLM Unique ID:
- 101734386 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101734386