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Expertise to Fit Your Specific Project Needs

Whether your aim is to obtain a CE Mark on your device or progress in your Medical Device Regulation (MDR) compliance journey, developing and maintaining compliant and standardized Clinical Evaluation Reports (CERs) is a critical component of any organization’s day-to-day operations. However, with consistent regulatory changes and shifting priorities, this involved, time-consuming process may not always be top of mind. That’s where Oxford comes in. Our CER solutions can be tailored to fit your needs, and our CER lifecycle-focused approach ensures you will come away with processes in place to update and maintain your CERs for years to come.

Comprehensive CER Experience

  • Subject Matter Experts
  • Literature Reviewers
  • Project Managers
  • Medical Writers
  • Technical Writers
  • QC Specialists

Areas of Service

  • Risk Mitigation
  • State of the Art Literature Search
  • Update of CERs
  • Protocol Development
  • Regulatory Compliant CERs
  • Utilization of Industry Best Practices
  • Standardized Process and Quality Control
  • Summary of Safety and Clinical Performance (SSCP)
  • Program Management to Successful Completion and Turn-Over

Systems & Software

  • End Note™
  • Distiller™
  • SharePoint™
  • Literature Search Databases: PubMed™, EMBASE™, and more
Quality Assured

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Supporting the Following Solutions

  • Clinical Evaluation Report Lifecycle
  • Final Planning
  • Writing
  • Quality Control
  • Completion Approval

Discover How Oxford’s Team
of Experts Completed Literature
Searches for CER Compliance

Quality Assured

Tell Us About Your Project