Understanding Europe’s New Clinical Trial Regulations

Learn more about the purpose of EU-CTR and uncover best practices for adapting to its requirements, with insights from the experts at Certara. You will gain a deeper understanding of these regulations and the requirements of using its CTIS to submit, assess, authorize, supervise, and report on clinical trials in the EU.

Read now to:

Understand the goals of EU-CTS and timeline for transitioning to CTIS use
Explore best practices for adapting to a role-based system
Explore clinical trial anonymization and redaction methods
Improve patient engagement and stay in EMA compliance by utilizing plain language summaries (PLS)
Understand critical importance of proactively and accurately planning timelines under EU-CTR

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