Preparing for the Clinical Trials Regulation (CTR)

Regulatory Factsheet

Preparing for the Clinical Trials Regulation (CTR)

The CTR (Regulation (EU) No 536/2014) replaces the EU Clinical Trials Directive and local implementing legislation and provides the requirements for conducting clinical trials in member states of the European Union (EU). For more information on preparing for the CTR, download the 2-page factsheet below.

For more information on how the Boyds team can support your drug development project, get in touch.

February 14, 2024

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Regulatory Factsheet

Preparing for the Clinical Trials Regulation (CTR)

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