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EU Clinical Trial Regulation Summit

Understand Impending Changes for Harmonised Submission and Assessment Requirements

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Who should attend?

You will benefit from this event if you have responsibilities in Clinical Operations, Trial Disclosure, Regulatory Disclosure, Clinical Transparency, Clinical Trial Regulation, CRS, Medical Writing or Biometrics and Reporting

Details

The scope of the CT Regulation is extensive; ensure your organisation effectively implements this new prevision at CBI's EU Clinical Trial Regulation Summit, where you will have the opportunity to connect with leading clinical experts and colleagues to ascertain critical updates on regulatory requirements and discuss the most efficient approaches for clinical trial compliance. For more information on sessions and faculty lineup, view the complete programme at cbinet.com/ClinicalTrialsEU or contact Stuart Steller via telephone, +1.339.298.2158, or email, stuart.steller@cbinet.com.

Contact

Stuart Steller
stuart.steller@cbinet.com

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