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Academic Credit for Data Sharing
Balancing Data Anonymization with Data Utility
Causality training
China Global Regulatory Program
Data monitoring committees
Good Clinical Practice (GCP) and Multi-Regional Clinical Trials (MRCT) Training
Harmonized Governance Tools for Data Sharing
Health Literacy in Clinical Research
India Regulatory
Clarifying Data Sharing in Informed Consent
Bioethics Collaborative
Post-Trial Responsibilities
Clinical Research Professional Competency
Protocol Ethics
Real World Evidence
Representation of Diverse Populations
Research, Development, and Regulatory Roundtable (R3) of the MRCT Center and Ropes & Gray LLP
Return of Individual Results
Return of Aggregate Results
Global Clinical Trial Data Sharing
See All Resources by Project
Research, Development, and Regulatory Roundtable (R3) of the MRCT Center and Ropes & Gray LLP
Focus Area:
Ethics, Conduct, and Oversight
Proceedings, Publications, & Public Comments:
Comments to EDPB on the Guidelines on the Territorial Scope of the GDPR (Public Comments)
Other Resources:
Research, Development, and Regulatory Roundtable (Info Sheet)