Proscizen’s medical monitoring expertise includes –

1. Creation of medical monitoring plan
2. Training of project team  and resolution of project specific procedural problems
3. Medical review and interpretation of clinical data and documents including but not limited to Protocol, CRFs, Informed consent forms, safety narratives, clinical study report
4. Medical interactions with Proscizen project team, sponsor, and site clinical staff
5. Medical review of data after data entry

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6. Medical review and reporting of safety-related events
7. Other medical activities on behalf of sponsor