Clinical

Retroscreen Virology offers a complete clinical trial service from Protocol/Case Report Form design through to effecting and co-ordinating the study and soon hopes to expand into data management and monitoring. We have been conducting clinical trials for the past 11 years. Our group has extensive knowledge encompassing phase II to IV studies, which are all conducted according to International Conference on Harmonisation/Good Clinical Practice (ICH/GCP) standards. These studies include:

  • Human Influenza Challenge studies
  • Prophylactic trials with influenza neuraminidase inhibitors
  • Therapeutic trials with influenza neuraminidase inhibitors
  • Influenza vaccine trials (intranasal or intramuscular)
  • Common Cold studies

All trials are subject to independent assessment and approval by the Local Research Ethics Committee/Multi Research Ethics Committee (as appropriate); the application procedure for which is included within our service.

If you want to know more about our services in this area please click here to contact us.