Medical Devices in the EU: CE Mark and 93/42/EEC Directive 2010
16 Sep 2010
Online Event
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.
Past Events
Medical Devices in the EU: CE Mark and 93/42/EEC Directive 2010 - 16 Sep 2010, Online Event (7991)
Medical Devices in the EU: CE Mark and 93/42/EEC Directive 2026
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
