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GDPR in Clinical Research

The new guidelines issued by the European Data Protection Board published in January 2019 have been the source of many questions and interpretations of GDPR principles in the context of their applicability and daily use in the clinical research field.

This training aims to explain in-depth the legal basis for processing personal data in the context of clinical trials, such as legal obligation, consent, a task carried out in the public interest or legitimate interest and the legal basis for using clinical trials data outside of the trial protocol.