📄️ 2.10.1 Meetings - Trial Management
In this section, enter information about meetings that are undertaken by trial management staff, such as total number of meetings, average number of attendees and the travel information for those attendees.
📄️ 2.10.2 Meetings - Monitor Visits
A monitor visit is when the trial sponsor or a third party visits the trial site to perform quality control measures such as verification that the study protocol is being adhered to, or checking that informed consent is appropriately documented. These visits are usually performed throughout a trial’s duration and conducted in the form of a meeting.
📄️ 2.10.3 Meetings - Investigator Meetings
An Investigator visit or meeting is when visits are conducted to the research site to ensure the study is set up, conducted, and closed out in compliance with the protocol, regulatory requirements, and good clinical practice (GCP).
📄️ 2.10.4 Meetings - Ethics Meetings
Ethics committee meetings are conducted to review and evaluate the ethical aspects of proposed trials. These meetings are conducted independently of the trial sponsor or investigators.
📄️ 2.10.5 Other Meetings
This section can be used to enter information about any other meetings that occurred which were related to the trial. (This does not include Trial Management meetings, Monitoring Visits, Investigator Meetings and Ethics Meetings)