Our third Privacy Pill focuses on a critical phase in clinical trials: the proper definition of roles, obligations, and responsibilities of all stakeholders involved in patients’ data processing activities (sponsors, research centers, investigators, CROs, laboratories, depots, and other subcontractors).
Properly defining privacy roles in clinical research is crucial for data protection, as well as for compliance with data protection laws and regulations.
Stay tuned for more Privacy Pills to deepen your understanding of privacy in clinical research.
