§287d–1 National data system and clearinghouse on research on women’s health

Summary

The NIH Director, working with the Director of the Office and the Director of the National Library of Medicine, must create a public data system to collect, store, analyze, find, and share information about women’s health research done or supported by the national research institutes. It must be available to health care providers, researchers, and the public and include a clinical trials registry showing eligibility, sex, age, ethnicity or race, and trial location. Principal investigators must give that information within 30 days after it is available and must report trial results, including any toxicities or adverse effects, when the trial is completed. The NIH Director, with the same partners, must also set up and run a program to provide information on the institutes’ women’s health research and prevention activities.