specialty projects
The swift, short-term help you need to get over the hump.
At Courante Oncology, we can also provide experienced, well-trained clinical trial resources to help ease your short-term work crunch and meet impending deadlines. And without any long-term commitments or contracts! Turn to us for:
Clinical monitors to conduct “emergency” source review and data retrieval for:
Supplemental data management support to clinical sites to help:
Help with review and collection of regulatory documents to:
Short-term medical writing resources for:
Quick feasibility studies to help determine potential opportunities and realistic project timelines
At Courante Oncology, we can also provide experienced, well-trained clinical trial resources to help ease your short-term work crunch and meet impending deadlines. And without any long-term commitments or contracts! Turn to us for:
Clinical monitors to conduct “emergency” source review and data retrieval for:
- Interim analyses
- Abstracts/posters
- Regulatory submissions that have extremely aggressive timelines
- FDA requests for supplemental data
- Sites with unexpected CRA turnover
- Investigator-sponsored trials that might provide data needed to make development decisions
Supplemental data management support to clinical sites to help:
- Meet unexpected study data collection deadlines
- High-enrolling sites meet aggressive timelines or catch up
- Bridge the gap that occurs with turnover of trained study staff
Help with review and collection of regulatory documents to:
- Ensure that site files are complete and current
- Ensure that all relevant and required information has been submitted to IRBs
Short-term medical writing resources for:
- "Old" study reports that never seem to get concentrated resources
- Updating investigator brochures quickly
- Abstracts/posters
- IND/NDA Annual/Periodic Reports
- Writing safety narratives
Quick feasibility studies to help determine potential opportunities and realistic project timelines
