WebA secure collaboration environment for sharing and exchanging clinical trial master file content with both internal teams and external contributors (i.e., sponsors, CROs, study sites, etc.). System notifications that are triggered after trial master file checklist milestones have been met and/or when task assignments have been completed. WebThe Regulatory Binder is often the first document reviewed during audits and inspections. Not all the essential documents are available at the start of the study. Documents can be grouped into those that are generated before study initiation, those that are generated during trial conduct and those that are generated after study completion.
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