Medical Devices in the EU: CE Mark and 93/42/EEC Directive 2010
September 16, 2010(Ended)Web conference
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.
Prices *
249 US Dollar
Exhibition
No exhibition
Organization
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
Articles/News/Press releases
- Mechanisms of hearing loss in prematures and fullterms with perinatal or postnatal hypoxia
- Effect Of Traditional Egyptian Herbal Medicine on Treatment of Hepatitis C virus (HCV)
- Business conference and trade shows as an efficient tool
- Determine the prevalence of hypermetropia among young male and female
- Aspects of business development through a business conference or exhibition
- Cochlear Implantation in Auditory Neuropathy
