When you work with Qserve CRO, you can benefit from our broad experience across numerous therapeutic areas. Since 2017, we have been involved in more than 30 studies, across a range of therapies, and complex study designs. We tap into this experience in every project.
Qserve CRO believes in setting-up clinical trials tailored to your medical device-specific needs. Our clinical team gained experience working at Notified Bodies, CRO’s and sponsors/manufacturers. This combination of different backgrounds, combined with Qserve’s in-depth knowledge of regulatory affairs creates efficient and compliant clinical trials.
Our expertise is a full-scope service for pre-market and post-market studies from class I to class III. Qserve understands the operational and financial challenges involved in conducting clinical trials for medical devices.