European clinical studies and literature-based clinical evaluations for medical devices since 2005
As a contract research organization (CRO), CERES can help you solve your problems and meet your goals, both before and after demonstrating CE conformity. We offer complete clinical trial management for medical devices, as well as just the help you need to succeed. We can fulfil the ongoing regulatory responsibilities necessary to gain and maintain your CE mark. We also perform market surveillance via Post-Market Clinical Follow-up (PMCF) studies. All of our services can be customized to fit your needs.
In 2005, Dr. Stephan Joeken founded CERES, foreseeing increasing requirements for clinical trials on medical devices in Europe.
At CERES evaluation & research GmbH, our comprehensive understanding of these past and potential regulatory changes and our proactive project management style has led to our success. Especially for long-term clinical trials, early consideration of regulatory changes is important.
CERES evaluation & research GmbH has performed clinical studies in several European nations, and has achieved CE approval for numerous medical devices via literature-based clinical evaluations.
In the future, we hope to share our success with you.