Medical Monitoring / Pharmacovigilance

Clinicology pharmacovigilance support can be integrated into the trial offering or stand alone. 

Activities include:

• Medical monitoring for trials
• 24/7 cover if required
• Strategic medical review of protocols or development plans
• Safety Management Plan Development
• SAE / SUSAR Processing, Submission, Reporting
• Case narratives
• Safety database development / maintenance
• DSUR production and submisison