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Publication and Clinical Trial Transparency

Data Anonymisation | Policy 0070 | U.S. Final Rule | GDPR | Lay Summary Preparation | Publication Strategy

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Who should attend?

You will benefit from attending this event if you are from a bio/pharmaceutical or medical device company with responsibilities or involvement in the following areas: Clinical Trial Transparency, Clinical Trial Disclosure, Publications Scientific Information/Communication, Data Anonymisation, Data Transparency/Data Privacy, Medical Writing, Clinical Information, Clinical Trial Registration, Medical Affairs

Details

In its 7th year, Publication and Clinical Trial Transparency creates a bridge between the key stakeholders from clinical trial transparency, disclosure, publications, data anonymisation and medical writing teams. Gather together to compare processes and exchange best practices in preparing and executing policy 0070 submissions, ensuring compliance with GDPR, understanding data anonymisation standards and building compliant processes in alignment with other global regulations including EU Clinical Trials Regulation and U.S. FDAAA Final Rule.

Join us at this critical time of change in the global clinical trials landscape to benchmark with peers on the ever-evolving transparency requirements and strategies for managing publications strategy to develop the most widely accepted and efficient best practices.

Prices

Register by 20 April 2018 and save €250

Contact

Evanna Payen
evanna.payen@cbinet.com

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