Year: 2024
Type: article
Abstract: This Viewpoint discusses the US Food and Drug Administration’s authority to require drug and device sponsors to submit diversity action plans and policy gaps that limit the organization’s ability to achieve demographic representation in clinical trials.
Source: JAMA
Authors: Tanvee Varma, Barbara E. Bierer, Andrew Hantel
Language: English
Topic: Ethics in Clinical Research
Field: Medicine
Domain: Health Sciences
SDG: Reduced inequalities
Open Access status: green
Awards: G4823681033, G9000011404
OpenAlex ID: W4402666334
