HEALTHCARE TRAINING 2020 - 6-Hour Virtual Seminar - The New EU Medical Device Regulation
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Website https://www.globalcompliancepanel.com/virtual-seminar/6-hour-virtual-seminar---the-new-eu-medical-de |
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Category HEALTHCARE TRAINING 2020
Deadline: August 19, 2020 | Date: August 19, 2020
Venue/Country: Online event, U.S.A
Updated: 2020-06-29 21:57:45 (GMT+9)
Call For Papers - CFP
In 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.This Seminar will look at what to expect when the new regulation is implemented. Including: the transition period, Effect on Notified Bodies, Impact of the MDR on Quality Management Systems (QMS), technical documentation, clinical trial requirements, UDI and combination products.Why you should attendBecause the current Directive will be significantly altered and replaced by a Regulation which is legally binding on all Member States.Who Will BenefitClinical Trial ManagersRegulatory AffairsMedical Officershttps://www.globalcompliancepanel.com/virtual-seminar/6-hour-virtual-seminar---the-new-eu-medical-device-regulation-11494LIVE
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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