MeDiNova’s principal aim is to deliver quality clinical trials data on time at its investigator sites. We have developed high quality standards and SOP’s which are strictly adhered to.
We undertake internal audits and are regularly visited by monitors from sponsors and CRO’s who are satisfied with our procedures. As MeDiNova are large recruiters of patients, we are regularly inspected as part of the Sponsors’ MHRA audits. MeDiNova is approved by the LREC and MREC authorities to undertake research studies.
We consider it vital to work with clear standard operating procedures (SOP’s). This ensures that the quality of our clinical research is consistently high and delivered in the same manner by all our team. Our teams adhere to the SOP’s and regular training is undertaken.