FDA releases guidance for remotely acquiring data in clinical investigations
The draft report offers recommendations for stakeholders about using digital health hardware and software to gather information from remote trial participants.
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The draft report offers recommendations for stakeholders about using digital health hardware and software to gather information from remote trial participants.
This week in Washington: President Biden acknowledges that the Build Back Better Act might not pass Congress this year.
Upcoming Hearings/Markups - December 8 - House Agriculture Committee, Nutrition, Oversight, and Department Operations Subcommittee Hearing: “Review of USDA...
Recently, the Food and Drug Administration issued a draft guidance, “Content of Premarket Submissions for Device Software Functions,” to help industry understand what it should include...
Congress - House - House Passes Reconciliation Package - On Nov. 19, the House passed the $1.7 trillion reconciliation package with a vote of...