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Two New Revised Common Rule Webinars Available: Revisions to Definitions and Revisions to Informed Consent

Add our newest revised Common Rule webinars covering the revisions to definition and revisions to informed consent. They are ideal for IRB member human subject protection staff, and other members of the research team.

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Two New Revised Common Rule Webinars Available: Revisions to Definitions and Revisions to Informed Consent

Recent News

Laboratory Chemical Safety Available in Audio-Visual Format New Webinar Available: Building a ClinicalTrials.gov Compliance Program – Tips for Investigators and Institutions New Course Available: Compensation Reporting (Effort Reporting) Explore New Content (July - December 2019) New All Access Webinar Package Available CITI Program Account Checkups Payment Portal for Credit Card Payments New Webinar Available: Preparing for Single IRB (sIRB) under the Common Rule Associate Director of Educational Initiatives, Margaret Rankovic's Contribution to Health Literacy New Course Available: IACUC Administration New Dynamic Content Format New Webinar Available: Ethics & Policy Issues in CRISPR Gene Editing New Webinar Available - Research with Native American Communities: Important Considerations When Applying Federal Regulations New Course Available: Laboratory Chemical Safety Important Change of "Site" Definition for Organizational Subscriptions FDA Issues Guidance on Live Case Presentations During Investigational Device Exemption (IDE) Clinical Trials Apply for the 2019 Dr. Paul Braunschweiger Annual Scholarship Program