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| Competent site monitoring is critical to ensure the integrity of the study data and adherence to regulatory requirements. At Veeda Oncology®, we take great pride in the knowledge and breadth of experience of our field monitors. All
monitors must have a strong
oncology background; many of our monitors have more than 10 years experience monitoring in the oncology arena. We strongly encourage CCRA certification and monitors are involved in ongoing training. Because of the strength of their monitoring skills, our monitors are better able to identify and address potential problems. |
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| Veeda Oncology offers a number of monitoring services: |
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- Development of monitoring plans
- Development of monitoring tools for improved consistency and efficiency while on-site
- Development of monitoring report templates per sponsor specifications
- Development of site feasibility questionnaires
- Identification of study investigators
- Site qualification visits
- Site initiation and training
- Interim monitoring visits
- Review and collection of regulatory documents
- Close-out visits
- Drug accountability
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| We believe that a cohesive team – site personnel, CRO and sponsor – are necessary to successfully complete
clinical trials and ultimately get new drugs to market. Our
monitoring staff understands that excellent site and sponsor relationships, open communication and a proactive approach to
monitoring lead to quality data. |
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