Clinical Evaluation Reports (CER`s) Required for All Medical Devices in Europe 2016 is a webinar that covers topics such as:
- Prepare and execute a literature review
- The Essential Requirements and the relationship to the CER
- Construct and manage the Technical File
- The elements comprising the CER and recommended format
- What resources exist to guide you in developing a clinical evaluation report , including how to select a format for writing it and keeping it updated
- The expectation that devices sold in Europe must have a CER in it`s Tech File unless you justify otherwise
Clinical Evaluation Reports (CER`s) Required for All Medical Devices in Europe 2016 is intended for attendees from:
- Regulatory Affairs Management and RA Specialists
- QA/Compliance
- Consultants
- Marketing
- Clinical Affairs