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The Multi-Regional Clinical Trials Center of Harvard and Brigham and Women's Hospital
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SubNav: Resources

  • Resources Overview
  • Academic Credit for Data Sharing
  • Advancing the Quality of Clinical Trial Enterprise
  • Balancing Data Anonymization with Data Utility
  • Bioethics Collaborative
  • Causality training
  • China Global Regulatory Program
  • Clinical Research Professional Competency
  • Data monitoring committees
  • Good Clinical Practice (GCP) and Multi-Regional Clinical Trials (MRCT) Training
  • Health Literacy in Clinical Research
  • Impact of GDPR on Clinical Research
  • India Regulatory
  • Post-Trial Responsibilities
  • Proactive Safety Surveillance: A Global Approach
  • Promoting Global Clinical Research in Children
  • 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
  • Tools for Data Sharing
  • Global Clinical Trial Data Sharing
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China Global Regulatory Program

Focus Area: Global Regulatory Engagement

China Global Regulatory Program

Proceedings, Publications, & Public Comments:

  • Comments to China FDA on resolving the backlog, Chinese Translation (Public Comments)
  • Comments to China FDA on resolving the backlog (Public Comments)

Presentations:

  • Multi-Regional Clinical Trials (MRCTs): Practice and Issues of Multi-Regional Clinical Trials’ Global Acceptance (Presentation – Login required)

Sponsor Resources:

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The Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard

14 Story Street, 4th Floor, Cambridge, MA 02138, USA

Telephone: (617) 496-9807

Email: mrct@bwh.harvard.edu

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