At MeDiNova we differentiate ourselves by providing a personal service to clients in our ‘‘MeDiNova Way’’.

We devote significant effort to developing our Global Network of Quality Research sites. We provide them the following:

  • Business development, budgeting and contracting
  • Site selection, start up and ethics submissions
  • Recruitment beyond their database
  • Program management and escalation
  • Operational Compliance reviews and quality audits
  • Retention activities and training on patient experience
  • General development of the clinical research activities at site level

The result of our extensive and hands on approach at sites means that our pharma and CRO clients benefit from an outstanding performance from our trials. 

We are committed to making sure that we work with you from project conception, through to completion, to deliver a comprehensive and efficient trial


Contact Research Organisations (CROs)

MeDiNova provides CROs with opportunities to recruit large volumes of high quality patients at identified strategic sites. By consolidating efforts through a focused approach and utilising experienced staff we manage the study to deliver the desired outcomes.


Quality is a core value of MeDiNova and at the centre of everything we do.  We have a highly skilled quality team who are dedicated to ensuring that all our procedures are streamlined and robust.  

Our methodological procedures, controls, metrics and training comply with regulatory and ethical ICH GCP requirements and standards to ensure the accuracy of patient data.   

Experienced quality staff and auditors ensure consistent best practice is consistently maintained and that excellence is reflected by our clinical teams throughout all our investigator sites.