Courante Oncology
  • Home
  • About
    • Client Benefits
  • Services
    • Specialty Projects
  • Experience
  • Careers
  • Contact

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

We welcome the opportunity to discuss your needs or answer any questions you may have about our company or services. Contact us today or complete our inquiry form and we'll get back to you as soon as possible. 
Submit
Picture
©2023 Courante Oncology  |  Privacy Policy | Contact Us
  • Home
  • About
    • Client Benefits
  • Services
    • Specialty Projects
  • Experience
  • Careers
  • Contact