A detailed feasibility analysis is conducted by a dedicated feasibility team. We directly contact potential investigators in all countries under consideration. We provide a comprehensive report detailing the suitability of the protocol design for implementation by research sites as a whole and in each individual country. Also provided are accurate country and site selection data, insight to regulatory requirements, assessment of competitive trial impact, and risk mitigation strategy coupled with a precise budget and timeline forecasts. This information is complimentary and without obligation, it is given to our clients during the proposal stage. Our confidence in the accuracy of our Feasibility Plus™ process enables us to guarantee study start-up time to enrolment.
One Trial One PriceTM
We believe sponsors should be able to rely on cost proposals and should not be subject to numerous change orders after contract signature. With confidence in our expertise in organising, managing, and executing clinical studies, we offer the following pledge: the price agreed at contract signature is the price you will pay. This allows us to offer our clients a concrete budget, something not typically seen in the change order culture of today’s CRO industry.
Operational Excellence - Quality By Design
Reputed for its customer focus, flexible approach and strong project management, CROMSOURCE has an 80% level of repeat business. Since 1997, we have worked in Western Europe, the Central & Eastern European regions, Russia & Ukraine. We know these places intimately and our depth of experience enables clients to include them confidently in their clinical studies. 'Quality by Design' is our process for ensuring close management of all operational aspects with an eye toward proactive identification and prevention of an integrated, certified ISO 9001 quality system first awarded to us nearly 20 years ago.
Guaranteed Date for Database Lock
We have proven by experience that if you assess feasibility realistically, enrol and start on time, and conduct the clinical study with scientific and managerial discipline; the study can be completed on time and on budget. And if this is the case there is no reason not to guarantee a date for Database Lock. Confidence in our operational processes enable us to make this pledge.
Via Giorgio De Sandre, 3
37135 Verona - Italy
Direct: +39 045 8222811
North American Headquarters:
8000 Regency Parkway, Suite 575,
Cary, NC 27518 – USA
Direct: +1 919 626 9882
ISO 9001:2015 multi-site certified quality management system
ISO 14155:2020 conformity confirmed.
|CROMSOURCE End to End Guarantee Fact Sheet.pdf||Download|