MeDiNova works with the leading pharmaceutical, biotech and Contract Research Organisations (CROs) and establishes long term mutually beneficial relationships.
Our aim is to provide pharma clients with a high value service in the delivery of clinical research at investigator sites.
We provide global reach focusing on targets being achieved in collaboration
We are committed to making sure that we work with you from project conception, through to completion, to deliver a comprehensive and efficient trialCMO/MD
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.