LIVE Webinar - EU Clinical Trial Regulation: Applying CCI best practices to accelerate preparation of CTIS public version documents

A comprehensive review of the EMA guidance regarding CCI, best practices to operationalize and streamline your internal CCI identification and redaction processes including review of specific use cases and examples. This webinar will include audience Q&A.

Thursday, May 18th at 10am

Register on Zoom Here:


crossmenu linkedin facebook pinterest youtube rss twitter instagram facebook-blank rss-blank linkedin-blank pinterest youtube twitter instagram