The General Data Protection Regulation (GDPR) and Clinical Trials
The General Data Protection Regulation (GDPR) and Clinical Trials
To purchase access for your team, or if you have any questions, email us at info@clinicalpathwaysresearch.com.
Course outline HERE
INTERACTIVE DEMO AVAILABLE BELOW
This course covers the exchange of personal data from the European Union (EU) to the United States (US) while following the requirements of the EU’s General Data Protection Regulation. Content includes what is applicable to stakeholders in clinical trials, how to protect data subject personal information collected and analyzed in clinical trials, and impacts to clinical trials and your organization.
Course Length: 45 minutes
INCLUDES:
Unlimited access to the content for 45 days from your initial day of purchase.
Certificate of completion
Case Studies
Post-Assessment
Knowledge Checks
LEARNING OBJECTIVES
Determine the importance of subject data protection related to General Data Protection Regulation (GDPR).
Describe the process to collect and analyze private data and ensure its security under GDPR.
Recognize potential impacts of the GDPR and how it affects your organization.
AUDIENCE
All clinical research personnel
INTERACTIVE DEMO:
