The team’s primary focus is to generate analytical and clinical performance data to underpin the safety and effectiveness of the CytoCell® FISH products. The team is generating in-house data as well as recruiting clinical investigators and is planning and executing analytical and clinical trials and data collection activities. Working closely with the Regulatory Affairs team in Cambridge, the team is co-ordinating and providing reporting information for reports submitted in regulatory agencies.
The Medical Affairs scientists act as scientific liaisons and provide scientific and clinical input for in-house and external activities and are responsible for the QC analysis of the CytoCell FISH probes.
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