I am thrilled to announce our latest addition to the Eisner Safety Consultants team Mary Weick-Brady recently joined our team and will help us support a growing need for the Wearable Medical Devices and the Home Use Medical Markets. Ms. Weick-Brady comes with
AS/NZS IEC 60601.1:2015 (Edition 3.1) Just Published
Just Published on 23 Sept 2015 the Australian / New Zealand Joint Standard AS/NZS IEC 60601.1:2015 which is based on the complete IEC 60601-1, edition 3.1:2012 (identical). The only differences are in the AS/NZS IEC 60601-1:2015 the preface states to a) replace the international
Standards Reconnaissance Subscription Service Coming Soon
Does your Medical Device Regulator or your Quality System require that you maintain a list of applicable standards to meet these requirements for your product lines? How much time does it take to put this list together and how much
FDA Updates Guidance on Device Classes Exemptions from Premarket Notifications Requirements
This post covers 8 product codes added & updates made to the guidance on Device Classes Exemptions from Premarket Notifications Requirements On Aug 14, 2015 FDA updated the Final Guidance Document titled “Intent to Exempt Certain Unclassified, Class II, and
Back by Popular Demand – Wearable Medical Devices – FDA’s Current Thinking
As this presentation was so well attended in July FX Conferences has decided to rerun this presentation twice in August so those that missed it can obtain this critical information for the Wearable Medical Device industry. Leo Eisner will be
