Quality and Delivery to Pharma, Biotech and CROs are MeDiNova’s passion and we work tirelessly to achieve these aims.
Our quality record is maintained at a very high level and we support this through our extensive Operational Compliance reviews at site level.
Our Delivery record is exemplary, and we aim to be the highest recruiters on studies, whilst providing high quality in terms of data management, patient safety and information integrity.
In recent studies in Osteoarthritis, COPD, Vaccines, Osteoporosis, Migraine and Opioid Induced Constipation, MeDiNova sites have regularly featured in the Top 10 sites globally for the Pharma and CRO. We are very proud of these achievements.
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.