How Visby Achieved De Novo Marketing Authorization with Medrio CDMS/EDC
Learn how Visby achieved FDA De Novo authorization using Medrio CDMS/EDC – submitting their application just 45 days after the final participant’s visit.
Learn how Visby achieved FDA De Novo authorization using Medrio CDMS/EDC – submitting their application just 45 days after the final participant’s visit.
In this case study, see how Clinilabs supports quality data and efficient supply chain management with Medrio CDMS/EDC and RTSM.
In this case study, see how Insightec increased study speed and data accuracy for their medical device clinical trials with Medrio CDMS/EDC.
In this case study, learn how Medrio’s dynamic, cost-effective solutions ensure high-quality data and operational excellence for CTRG.
Uncover how this CRO delivers high-quality results and accelerates study timelines for their sponsors’ clinical trials.
Sign up to have our the latest insights delivered to your inbox.