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Start Over Subjects Informed Consent ✖Remove constraint Subjects: Informed Consent

11. Live case presentations during investigational device exemption (IDE) clinical trials: guidance for institutional review boards, industry, clinical investigators, and Food and Drug administration staff

Publication:
Silver Spring, MD : Center for Devices and Radiological Health, July 11, 2019
Subject(s):
Clinical Trials as Topic
Device Approval
Data Collection
Ethics Committees, Research
Informed Consent
Single-Case Studies as Topic
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

13. Consent-to-share: California’s opportunity to modernize cross-sector data sharing

Author(s):
Franceschini, Robby, author
Leslie, Timi, author
Stein, Daniel, (Of California HealthCare Foundation), author
McCoy, Kristine, author
Pertman, Adam, (Of California HealthCare Foundation), author
Publication:
[Oakland, CA] : California Health Care Foundation, October 2023
Subject(s):
Access to Information
Confidentiality
Government Programs
Health Policy
Information Dissemination
Informed Consent
Intersectoral Collaboration
Medicaid
Quality Assurance, Health Care
State Health Plans
California