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Project
  • Publication
July 14, 2023
Terms and conditions apply: an ethical analysis of mobile health user agreements in research
Research, Development, & Regulatory Roundtable (R3) , Bioethics Collaborative , Oversight and Implementation of Decentralized Clinical Trials
  • Annual Report
December 15, 2022
2022 MRCT Center Annual Report
Advancing the Quality of Clinical Trial Enterprise , Data Sharing , Diversity, Inclusion, and Equity in Clinical Research , Health Literacy in Clinical Research , Post-Trial Responsibilities , Promoting Global Clinical Research in Children , Oversight and Implementation of Decentralized Clinical Trials , Bioethics Collaborative , Research, Development, & Regulatory Roundtable (R3) , Return of Aggregate Results , Return of Individual Results
  • Proceedings
December 14, 2022
MRCT Center 2022 Annual Meeting Proceedings
Data Sharing , Diversity, Inclusion, and Equity in Clinical Research , Research, Development, & Regulatory Roundtable (R3) , Training & Education
  • Public Comments
October 31, 2022
Comments related to 2005 PHS Policies on Research Misconduct
Research, Development, & Regulatory Roundtable (R3)
  • Publication
September 29, 2022
Hydroxychloroquine/chloroquine for the treatment of hospitalized patients with COVID-19
Real World Evidence , Research, Development, & Regulatory Roundtable (R3) , Bioethics Collaborative
  • Annual Report
December 7, 2021
2021 MRCT Center Impact Report
Advancing the Quality of Clinical Trial Enterprise , Data Sharing , Diversity, Inclusion, and Equity in Clinical Research , Return of Individual Results , Promoting Global Clinical Research in Children , Research, Development, & Regulatory Roundtable (R3) , Bioethics Collaborative
  • Publication
October 23, 2021
Demystifying Schrems II for the cross-border transfer of clinical research data
Impact of Privacy Laws on Clinical Research , Research, Development, & Regulatory Roundtable (R3)
  • Publication
September 1, 2021
Emerging ethical issues raised by highly portable MRI research in remote and resource-limited international settings
Research, Development, & Regulatory Roundtable (R3)
  • Publication
May 10, 2021
Mutual Recognition Of Physician Licensure By States Would Provide For Better Patient Care
Research, Development, & Regulatory Roundtable (R3)
  • Publication
March 8, 2021
Health Info Blocking Rule Creates Opportunities For Research
Research, Development, & Regulatory Roundtable (R3)
  • Annual Report
December 20, 2020
2020 MRCT Center Impact Report
Diversity, Inclusion, and Equity in Clinical Research , Promoting Global Clinical Research in Children , Health Literacy in Clinical Research , Bioethics Collaborative , Research, Development, & Regulatory Roundtable (R3) , Proactive Safety Surveillance: A Global Approach , Impact of Privacy Laws on Clinical Research , Training & Education , Joint Task Force for Clinical Trial Competency , Return of Individual Results
  • Publication
October 2, 2020
How to fix the GDPR’s frustration of global biomedical research
Impact of Privacy Laws on Clinical Research , Research, Development, & Regulatory Roundtable (R3)
  • Public Comments
September 28, 2020
Comments to European Data Protection Board Guidelines 04/2021 on Codes of Conduct as Tools for Transfers
Impact of Privacy Laws on Clinical Research , Research, Development, & Regulatory Roundtable (R3)
  • Public Comments
April 29, 2020
Comments to the European Commission on the Challenges that GDPR Raises for Research
Research, Development, & Regulatory Roundtable (R3)
  • Publication
March 2, 2020
Disruptive and Avoidable: GDPR Challenges to Secondary Use of Data
Impact of Privacy Laws on Clinical Research , Research, Development, & Regulatory Roundtable (R3)
  • Annual Report
December 4, 2019
2019 MRCT Center Impact Report
Global Regulatory Engagement , Real World Evidence , Impact of Privacy Laws on Clinical Research , Promoting Global Clinical Research in Children , Health Literacy in Clinical Research , Diversity, Inclusion, and Equity in Clinical Research , Bioethics Collaborative , Research, Development, & Regulatory Roundtable (R3) , Proactive Safety Surveillance: A Global Approach , Data Sharing , Advancing the Quality of Clinical Trial Enterprise , Training & Education , Joint Task Force for Clinical Trial Competency
  • Publication
July 12, 2019
Implementing Regulatory Broad Consent Under the Revised Common Rule: Clarifying Key Points and the Need for Evidence
Research, Development, & Regulatory Roundtable (R3)
  • Publication
February 1, 2019
Guidance Regarding Interaction Between GDPR and EU Clinical Trials Regulation Leaves Several Questions Unanswered
Impact of Privacy Laws on Clinical Research , Research, Development, & Regulatory Roundtable (R3)
  • Public Comments
January 18, 2019
Comments to EDPB on the Guidelines on the Territorial Scope of the GDPR
Research, Development, & Regulatory Roundtable (R3)
  • Annual Report
December 5, 2018
2018 MRCT Center Impact Report
Training & Education , Joint Task Force for Clinical Trial Competency , Diversity, Inclusion, and Equity in Clinical Research , Health Literacy in Clinical Research , Bioethics Collaborative , Research, Development, & Regulatory Roundtable (R3) , Data Sharing , Global Regulatory Engagement
  • Other
December 5, 2018
Research, Development, and Regulatory Roundtable Info Sheet
Research, Development, & Regulatory Roundtable (R3)