Medical Monitoring

Our medical staff consists of board-certified oncologists/hematologists who are available to provide medical oversight of clinical studies.

Medical monitoring consults towards:

• Study design, protocol review, review of CRFs, statistical analysis plans, and the preparation of final study reports, abstracts and manuscripts
• Interactions with regulatory agencies
• Recruitment of investigational sites
• Protocol presentation and training at investigator meetings
• Conduct of clinical trials (advice to investigators regarding eligibility requirements, visit schedules, dosing adjustments and toxicity assessment)
• Medical review of serious adverse events
• Preparation of prompt reports for the regulatory agencies