Beginners Guide to Global Data
Protection Regulation (GDPR) for Clinical Trials
To remain compliant, you need to understand how GDPR affects your clinical trial operations. This guide offers insight the main terms that can be used to help you better understand the language utilized throughout the GDPR documentation and understand your organization’s role within the regulation.
There is also a Q&A section sourced from the document titled, “Question and Answers on the interplay between the Clinical Trials Regulation and the General Data Protection Regulation” from the European Commission Directorate-General For Health And Food Safety.
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What you will learn:
Critical language utilized in GDPR documentation
How GDPR effects clinical trial operations
- What role your organization plays in GDPR
- Common Questions and Answers about how the interplay between the Clinical Trials Regulation and the General Data Protection Regulation
Florence helps research sites, sponsors, and CROs take their day back from paper by transforming Clinical Trials with electronic document workflows and remote site access - and none of that can be done without complying to all regulations.
The information compiled in this document is sourced from the General Data Protection Regulation (GDPR) information from Intersoft Consulting and from the European Commission Directorate-General For Health and Food Safety.