Trial Coordinating Center (TCC)

The Trial Coordinating Center (see WP schema) will be responsible for coordinating the day to day running of the clinical trial and development of all study documentation, SOPs and the manual of operations, which will be reviewed and approved by Steering Committee and the ESRG. All approved critical study documents will be maintained in the clinical trial masterfile at the TCC. The TCC will be responsible for generating all approved revisions of study documentations and for version control.