Conference 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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