SAFETY & REGULATION

Medtech startups hear dour diagnosis

Posted by on December 10, 2011 at 9:57 pm

Medtech startups hear dour diagnosis¬†- by Rick Merritt, EETimes Here’s another angle on the BIOMEDevice Conference that I wrote about a few days ago, which expands on the points about regulation and VC investment trends. – Ken

BIOMEDevice San Jose 2011 – Trip Report

Posted by on December 8, 2011 at 1:53 am

- by Ken McGary, KSF Labs New international safety standards for medical equipment are on the way, namely revised IEC 60601 software validation and testing requirements, so Tuesday and Wednesday I attended the BIOMEDevice San Jose conference to get up to speed. Here’s a good background article on the new rules, which extend the concept […]