The Emergo Group issued a White Paper on 22 October 2012 in regard to the 26 September 2012 Proposed New Medical Device Regulations for Europe (this weblink brings you to the “Medical Devices – Ongoing Revisions” page of the EUROPA website).
L. Eisner Talk 13 Dec on IEC 60601-1, 3rd ed. – US, EU, Japan, Brazil, & Canada National Implementation
Leo Eisner will be speaking on “IEC 60601–1, 3rd Edition – Where Do We Stand on National Implementation?” via FX Conferences on Dec 13, 2012 at 11:00AM – Noon (Pacific), 2:00PM – 3:00PM (Eastern). He will be discussing the National
Medical Devices Utilizing Tissues of Animal Origin New EU Commission Regulation
This post is on the newly published Commission Regulation (EU) No 722/2012 of 8 August 2012 “concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured
Impact of WEEE2 on Medical Devices Industry
EUCOMED on 25 July 2012 wrote a nice summary of the Impact on the Medical Devices Industry of the long awaited revision of the Waste Electrical and Electronic Equipment (WEEE2 or WEEE recast) Directive (2012/19/EU) was published in the EU
Eisner Safety Consultants to Restart Monthly Newsletter Service
It has been over 2 years since we sent out our last newsletter. Our apologies. We have decided to send out a monthly update of our blog posts for each month which are all located at www.EisnerSafety.com/Industry_News/. We have been working