Federal health officials didn’t provide information on how people’s private medical data will be collected and managed.

Pritzker said the order was necessary in response to concerns about the creation of a federal autism registry or database without legal protections.

Federal health agencies are teaming up to create a powerful new research tool. The U.S. Department of Health and Human Services (HHS) announced plans to build a database of autism […] The post Federal ...

The director of the National Institutes of Health previously floated — then walked back — the idea of an autism registry, ...

Executive Order 2025-02 protects individuals from unauthorized data collection and sharing by state agencies and ensures that autism-related information is handled only when necessary and with ...

The partnership will focus first on "enabling research around the root causes" of autism spectrum disorder (ASD), HHS said.

Kennedy directed the health department to undertake a far-reaching research effort to identify the causes of autism, a ...

The U.S. Department of Health and Human Services on Wednesday unveiled a pilot program for the National Institutes of Health to tap into Medicare and Medicaid data in its search for the root causes of ...

The National Institutes of Health and Centers for Medicare and Medicaid Services Wednesday said Medicare and Medicaid private ...

The National Institutes of Health (NIH) and the Centers for Medicare & Medicaid Services (CMS) today announced a landmark partnership to enable NIH to build a real-world data platform enabling ...