Free Live Webinar – Understanding the New USG Policy for High-Risk Life Sciences Research
This webinar explores the scope of the new USG Policy for High-Risk Life Sciences Research.
10 events found.
Events
FDA’s Drug Registration and Listing Workshop: Compliance, Regulatory and Submission Updates
This workshop features updates from the FDA on establishment registration and drug listing submissions.
Free Webinar Replay – NIH Biospecimens Rule
Review how the NIH Policy on Enhancing Security Measures for Human Biospecimens tightens controls on sensitive personal data.
Free Webinar Replay – A Behavioral Approach to Compliance
Teaches how behavioral science can enhance compliance programs by exploring human decision-making drivers.
Free Webinar Replay – Being Creative when Applying the IRB Exemptions: Part 2
Discusses that IRB exemptions are underutilized because many institutions take a very conservative approach when applying them.
Free Webinar Replay – Seven Elements of an Effective Compliance Program: What Research Administrators Need to Know
Explores the seven key elements that ensure regulatory adherence, mitigate administrative risks, and promote ethical research administration.
Free Webinar Replay – Navigating the Intersection of Open Science and Responsible Conduct of Research
Serves as an introduction to open science principles and practices.
Clinical Center Ethics Grand Rounds: Ethics Of Reducing the Use of Animals In Research
Join the NIH for the "Clinical Center Ethics Grand Rounds: Ethics Of Reducing the Use of Animals In Research" session on October 7, 2026.
Town Hall – Biocompatibility and Toxicological Risk Assessment
Discuss toxicological risk assessments used to address biocompatibility endpoints for medical devices.
Beyond the Lab: Insights into Clinical Development in Pharma
Join the NIH for the "Beyond the Lab: Insights into Clinical Development in Pharma" workshop on October 7, 2026.