Development and Clinical

We are specialists in drug and device development requirements, including lab, non-clinical and clinical, as well as acting as a CRO.

  • Working with your CDMO
  • Working with your CMOs
  • Management of outsourced testing
  • Management of non-clinical studies
  • Facilitation of technology transfer
  • Writing and review of technical protocols and reports
  • CRO for clinical trials
  • Data management and biostatistics
  • Medical writing
  • ICH, ISO and local requirements
cta-bg
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Ann Handley

Ready for growth?

Contact us today and let's work together to achieve your goals. Whether you have a question, need more information, or want to discuss your project, our team is here to help.Let's talk
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