|
| |
| 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 of experience monitoring in the
oncology arena. We strongly encourage CCRA
certification and monitors are involved in
ongoing training. Because of the strength of
their skills, our monitors are better able to
identify and address potential problems. |
| |
| Veeda Oncology offers a number of monitoring services: |
| |
- 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
|
| 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. |
| |
