Clinical Trial Management
QCTR have an extensive network of contacts within GP Practices, hospitals and universities as well as within other CROs and consultancies. Through this network QCTR can execute a complete clinical trial from set-up through to clinical study report while retaining the ability to deliver core skills at an operational level, and in particular retaining control over the quality of the work being conducted. QCTR can execute a multinational clinical trial by partnering with other CROs in the countries where we do not have a base, but continuing to lead and manage the overall project within the QCTR structure. The QCTR team has extensive experience in working in precisely this manner within a virtual pharmaceutical company.
QCTR specialise in the therapeutic areas of psychiatry and neurology. As a small CRO, QCTR can respond quickly and flexibly to a sponsor’s needs. All services provided are conducted to the International Conference on Harmonisation’s guidelines for Good Clinical Practice (ICH GCP).
Clinical trial management services provided are as follows:
