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MDD Road shows: Regulatory framework of Medical Devices on its way One thing is clear: the requirements of the new EU Directive 2007/47/EC will soon come into effect. As of March 21, 2010, the new provisions must be applied - without any transitional periods or extensions. Yet the impact of this on the conformity assessment procedures as per Directives 90/385/EEC (active implantable medical devices) and 93/42/EEC (medical devices) is still unclear to many of the parties involved. TÜV SÜD's Road Shows offer a 1-day, high-caliber lecturer to inform you about the following issues: - What changes will the new Directive involve? - What must be implemented, and by when? - What will be changed in TÜV SÜD audits? - What to expect in the future?
Who Should Attend: Cost includes presentation materials and lunch. Scheduled Dates: Cost: $199.00 (USD) Time: 9:00 a.m.- 5:00 p.m.
Questions? contact:
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