DGCG

HHS/NIH proposed changes for registering, reporting clinical trial information

Today, the U.S. Department of Health and Human Services (HHS) issued a Notice of Proposed Rulemaking (NPRM), which proposes regulations to implement reporting requirements for clinical trials that are subject to Title VIII of the Food and Drug Administration Amendments Act of 2007 (FDAAA). The proposed rule clarifies requirements to clinical researchers for registering clinical trials and submitting summary trial results information to ClinicalTrials.gov, a publicly accessible database operated by the National Library of Medicine, part of the National Institutes of Health.

Blog post – oh, what a year it was!

Cartoon of four people in conversation.

During the fiscal year 2014, NIA was affected by a number of events and challenges. As the fiscal year winds down, Dr. Robin Barr, director of the Division of Extramural Activities, looks back on the changes and surprises that occurred, including an expanded research agenda, a budget increase, and an unexpected influx of well-written applications.

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