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Session 9: Protecting Confidential Information in Summaries of Trial Results
Session Chair(s)
Robert Paarlberg, MS
Principal
Paarlberg & Associates LLC, United States
Global clinical data disclosure and transparency requirements and initiatives have resulted in massive amounts of clinical data in the public domain. Local county and regional data protection regulations safe guard personal identifiable information from public disclosure. This session will explore how patient identifiable data are being protected in this global clinical disclosure/transparency ecosystem.
Learning Objective : At the conclusion of this session, participants should be able to:- Discuss the interplay between disclosure/transparency requirements and country/regional data protection regulations
- Identify stakeholder perspectives
- Implement best practices
Speaker(s)
Protecting Confidentiality: Public and Patient Perceptions and Best Communication Practice
Behtash Bahador, MS
Center for Information and Study on Clinical Research Participation (CISCRP), United States
Director, Health Literacy
Common Challenges Under GDPR for Data Disclosure and Transparency
Michael A. DiMaio, JD
Ropes & Gray LLP, United States
Attorney
Anonymisation and Public Trust (Remote Presentation)
Brendan Barnes
EFPIA, Belgium
Director, Data Protection & IP