April 2015
MassMEDIC Women in MedTech Forum: Disruptive Technologies in Medicine-Kick-off Event
MassMEDIC's Women in MedTech Forum's mission is to unite New England medical device executive women by providing an inspirational and educational leadership forum. Special Guest: Robin Strongin, President & CEO of Amplify Public Affairs (a woman-owned small business), and Creator & Founder of the award winning Disruptive Women in Health Care Join us for breakfast, great networking and the kick off meeting of the MassMEDIC Women in Medtech Forum. Meet Robin Strongin, founder of Disrupti"e Women in Health Care. The…
Find out more »August 2016
Software Development for Medical Device Manufacturers
MassMEDIC is sponsoring a two-day course titled Software Development for Medical Device Manufacturers on August 2-3 2016 at the Mass. Medical Society, 860 Winter Street, Waltham MA. Click on the course title for the course outline, registration and hotel info. Software Development for Medical Device Manufacturers An intensive two-day course... Developing software in compliance with the FDA Design Control regulation, guidance documents and international standards is challenging. This two-day intensive course provides practical solutions and suggestions for developing software in…
Find out more »June 2017
Med-Tech Talent Summit
A half-day seminar developed for C-level and HR executives from large multi-nationals to emerging technology start-ups. Companies will walk away with today’s most valuable tactics and strategies that you will be able to deploy immediately in your talent acquisition practices. Individuals will gain tremendous insight as to how best position themselves in a competitive job market and will learn methods to ensure that their backgrounds stand out and gain more attention. Topics for Discussion: Talent acquisition strategies & tactics in…
Find out more »August 2017
MassMEDIC presents: Two-day seminar – Software Development for Medical Device Manufacturers, August 2-3 2017
Developing software in compliance with FDA, EU regulations and international standards is challenging. This two-day intensive course provides practical guidance and suggestions for developing software that complies with applicable FDA and EU regulations, FDA guidance documents related to software and international standards including IEC 62304 and ISO 14971. The focus of this course is interpreting the FDA QSR regulation and guidance documents for software. Each section of the FDA Design Controls regulation (820.30) is discussed from the software perspective along…
Find out more »July 2018
MassMEDIC presents: Software Development for Medical Device Manufacturers
MassMEDIC is sponsoring a two-day course titled Software Development for Medical Device Manufacturers on Jul 31-Aug 1 2018 at the Mass. Medical Society, 860 Winter Street, Waltham MA. Click on the link below for the course outline, registration and hotel info. Software Development for Medical Device Manufacturers An intensive two-day course... Developing software in compliance with the FDA Design Control regulation, guidance documents and international standards is challenging. This two-day intensive course provides practical solutions and suggestions for developing software…
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