New EU Medical Device Regulation | Updated Regulation 2018
Added by globalcompliancepanel on 2018-03-20
Conference Dates:
Start Date: 2018-05-17Last Day: 2018-05-18
Deadline for abstracts/proposals: 2018-05-17
Conference Contact Info:
Contact Person: NetZealous LLC DBA GlobalCompliancePanelEmail: [email protected]
Address: Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Zurich, 1211, Switzerland
Tel: 800-447-9407
Conference Description:
Regulation proposals of the European Commission BackgroundIn 2012, the Commission adopted a package of measures on innovation in health. The package consisted of a Communication and two regulation proposals to revise existing legislation on general medical devices and in vitro diagnostic medical devices. In particular, the Directives on active implantable medical devices (90/385/EEC) and on medical devices (93/42/EEC) are intended to be replaced by a Regulation on medical devices, while the Directive on in-vitro diagnostic medical devices (98/79/EC) is intended to be replaced by a Regulation on the same subject. The revisions therefore affected all kinds of medical devices including in vitro diagnostic medical devices, from home-use items like sticking plasters, pregnancy tests and contact lenses, to X-ray machines, pacemakers, breast implants, hip replacements and HIV blood tests.
Location: Zurich, Switzerland Date: May 17th & 18th, 2018 and Time: 9:00 AM to 6:00 PM
Venue: Hilton Zurich Airport Hohenbuhlstrasse 10, 8152 Opfikon-Glattbrugg, Switzerland
Price:
Price: $1,695.00 (Seminar Fee for One Delegate)
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Until April 10, Early Bird Price: $1,695.00 From April 11 to May 17, Regular Price: $1,895.00
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