Courante Oncology
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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:
  • 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

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  • Home
  • About
    • Client Benefits
  • Services
    • Specialty Projects
  • Experience
  • Contact