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Popular pages
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About Us - CERES
As a contract research organization (CRO), CERES addresses your goals and requirements on medical devices, both before and after demonstrating CE conformity. We offer the complete management of clinic...
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Clinical Investigations - CERES
Clinical Investigations Need a clinical trial for a medical device in Europe? Would you like to use and improve your medical technology under controlled conditions? CERES can help you to access the Eu...
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Medical Writing - CERES
Medical Writing Medical Writing CERES has extensive medical device experiences within Regulatory, Quality and Clinical Affairs. Devices from class III to I, implants and active implants are subject of...
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Resources - CERES
MDR Checklist for the Clinical Product Lifecycle The following checklist gives an overview of the required documents essential as per MDR for a precise implementation of the clinical product lifecycle...
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IVD Performance - CERES
Approach In vitro diagnostic medical devices make a significant contribution to treatment control and diagnostics. Consequently, it is important to evaluate IVD devices performance and usability, so t...
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Post-Market Clinical Follow-up - CERES
Post-Market Clinical Follow-up Does your device already have CE approval? We help you collect targeted clinical data about your medical device by means of proactive Post-Market Clinical Follow-up meas...