Medical Devices in the EU: CE Mark and 93/42/EEC Directive 2010

  • 16 Sep 2010
  • Online Event

Description

This webinar will provide valuable assistance and guidance to all regulated companies that are preparing for CE Mark and ensuring compliance to MDD 93/42/EEC.

Areas Covered in the seminar:

  • Identify the steps required to obtain CE Mark and meeting compliance expectations.
  • Understand how to apply and use the Conformity Assessment Procedure.
  • How to classify your medical device correctly?
  • Learn how to use the Technical File correctly.
  • How to apply the Declaration of Conformity and why this is critical for success?
  • How ISO 13485 fits in with this process as a device company?
  • Learn and understand the expectations for the Essential Requirements and the Certification Process
  • How is the Authorized Representative involved and why and the ramifications of not meeting the requirements for CE Mark and 93/42/EEC for your company.
Note: Use this Promo Code(102924) to avail Discount of 10% on LIVE Purchase.

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Important

Please, check "Medical Devices in the EU: CE Mark and 93/42/EEC Directive" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Management, Marketing & Sales, Operations, Quality assurance
Education: Training
Health & Medicine: Medical device, Medical technology

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