Events

Discusses the confusion around CUI, including what it is, what it isn’t, and how universities and university research is impacted by it.

Discusses that IND safety reporting needs to be supported by ongoing systematic assessment of the product’s safety data from all sources.

Discusses how compassion fatigue, a form of secondary traumatic stress, affects animal care personnel due to exposure to distressing situations.

Offers a high-level overview of common risks in collaborative research environments and practical strategies to safeguard data and systems.

The HHS and the NIH SBPO will host a conference highlighting the current state of biomedical research at Historically Black Colleges and Universities.

This webinar series will highlight technical advances, translational insights, and future directions in synthetic biology and cancer research.

Join the OHRP on July 12 to explore the history and lasting significance of the Belmont Report at Belmont Manor & Historic Park.

Join the NIST for a multi-day workshop to discuss the Rapid Drug Analysis and Research (RaDAR) program.

Join the FDA for a virtual training on meeting federal requirements for clinical trial registration and results reporting on ClinicalTrials.gov.

This webinar will examine the BIOSECURE Act and its potential impact on research institutions.

The FDA will host a town hall to discuss the final guidance, Content of Human Factors Information in Medical Device Marketing Submissions.

Discussion of the importance of data privacy in the research field and best security practices to ensure compliance and research subjects' trust.