MeDiNova aims to revolutionise the clinical research industry by providing more access to Patients, helping Sites perform trials to a high standard of delivery and quality, and focus on timely enrolment at the best economic value for our Pharmaceutical and CRO clients.
MeDiNova works with healthcare systems and healthcare professionals to provide trial access to patients and also reaches out via social media and traditional outreach approaches. Our patient database is regularly provided with research study opportunities for potential participation.
Our Global Research Sites receive an unparalleled level of support to enhance their delivery capabilities. We support our Sites in business placement, negotiating budgets and contracts, study start up, staffing, programme management, training, operational compliance reviews and quality audits, retention strategies – all done in our unique “MeDiNova Way”, a hands on approach which yields extraordinary results and is welcomed by our Sites, Pharmaceutical and CRO clients, Regulatory Agencies and most importantly Patients.
We believe the continued development of the MeDiNova Way will serve as a key change agent for Site level operations within the Clinical Research Industry. Our aim is to set the new industry standard for Sites.