News

Is your organization prepared for a disaster? Have your Certified IRB Professionals (CIPs) finished their training? New LMS Interface Upgrades Coming Soon November 2018 Newsletter Recently Posted FDA Guidance Documents New Working with Genetically Modified Mice in Research Settings Course New Human Subjects Considerations and Big Data Research Module New and Updated Content New Bioethics Course Revised Common Rule: OHRP announces two public websites that will satisfy the consent form posting requirement Livestream - OHRP Exploratory Workshop: Meeting New Challenges in Informed Consent in Clinical Research OHRP Releases Draft Guidance Documents for Burden-Reducing Provisions During the Delay to the Revised Common Rule July 2018 Newsletter OHRP Guidance on the Effects of Disasters on Human Research Protections Programs Changing Organizational Affiliations and Transferring Completions CME/CEU Guidance for Administrators The FDA Will Require GCP Compliance for International Device Trials