Data on clinical trials become more accessible in Europe

18 June 2024
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In Europe, revised rules for the Clinical Trials Information System (CTIS) are now applicable, offering faster access to clinical trial information.

CTIS serves as the single-entry point for the submission and assessment of clinical trial applications in the European Union.

European regulators have introduced certain changes, with the goal of benefiting patients, healthcare professionals, and other stakeholders by providing earlier and more efficient access to clinical trial data.

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