Conducting a trial

MeDiNova specialise in managing trials effectively to deliver patients on a timely basis and conducting the trial activities to a high level of quality.

Our feasibility assessment process is a well informed and innovative process to achieve our clients’ requirements.

MeDiNova pride in having the lowest site startup times in the industry and our Programme Management team are relentless in the execution of the trial thereafter, all the way until database lock.

We recognise the utmost importance of quality and data integrity. We manage this by extensive Operational Compliance Reviews and Quality Audits during the life cycle of the trial.

MeDiNova also focuses on high patient retention during the study, this being achieved by providing excellent patient experience.

The MeDiNova Way ensures that we deliver the best outcome for our Pharma and CRO clients