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| Veeda Oncology Network, formerly International Oncology Network (ION-CR), is an innovative site management organization (SMO) with the capabilities to function as a full service Oncology specific Clinical Research Organization (CRO). The objectives of the SMO are to streamline the clinical trial experience by providing consistent administrative support to our practices. This practice support impacts the efficiency and effectiveness in providing clinical trial services to our pharmaceutical and biotech clients. In addition, we support our clients by providing decreased startup timelines through strategic development including project, regulatory and financial management.
Veeda Oncology functionality is supported by a group of professionals with extensive clinical trial knowledge as well as an average of 15 years of Oncology specific experience including site management, project management, regulatory, data management, monitoring, financial management, trial design, analytical, statistical, pharmacovigilance and medical writing.
The network is a group of independent community based Oncology practices across the U.S. operating as one large synchronized entity bound by a set of core operating procedures and values with 7 years of experience. With access to patients from over 100 locations, our 350 + experienced physicians and their qualified research staff are dedicated to conducting Oncology clinical trials. |
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| Mission Statement |
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| Veeda Oncology’s mission is to enhance the care of oncology patients through an uncompromising commitment to the standard of excellence in the conduct of oncology clinical trials. |
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| Distinguishing Features |
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| The following services we provide not only benefit our network practices but also our pharmaceutical and biotech clients. These benefits have been demonstrated over the past 7 years, through 55+ trials and greater than 1400 patients. |
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- Trial Design and Assessment
- Disease specific committee review
- Research Advisory Board review
- Investigator Initiated trial design
- Timely feasibility feedback
- Trial Start-up
- Master Clinical Research Agreement (MCRA) on file for each site
- Site selection support
- Site specific profile information provided upon request
- One budget and contract for all participating sites
- Central regulatory management
- Site initiation support
- Trial Operations
- Project management
- Site management
- Financial management
- Training
- Quality audits
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