Red Nucleus Training Institute

Providing on-demand training solutions

GDPR Requirements for Clinical Research Data

0.50 hrs | GDPR

This module will explore a range of topics that explain how GDPR applies to the processing and protection of clinical research data, including the lawful bases for processing personal data within the confines of a trial, related safeguards, clinical data autonomy under GDPR, and the balance between GDPR and HIPPA requirements.

Module Details

Over the next 30 minutes, we will explore a range of topics that explain how GDPR applies to the processing and protection of clinical research data, including:
• How GDPR defines clinical research data
• The lawful bases for processing personal and sensitive data
• Definition of data processing operations
• Data processing safeguard requirements
• Clinical data subject autonomy rights under GDPR
• How GDPR applies to clinical trial audit requirements and HIPAA regulations

Features

• Self-paced e-learning format
• On-demand access from your Learning Management
System (LMS) or from RN’s hosting solution, Unify
• Module-level interactive learning exercises and
self-check questions
• Fully cited and sourced from a blend of Red Nucleus
best practices and global health authority regulations
and guidance
• Updated annually
• SCORM compliant

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