Results 4 found
March 3rd, 2015
Designing for Compliance to IEC 60601-1 3rd Edition Workshop

Click here to register Description The medical device industry is the most heavily regulated in manufacturing, for good reason. Devices that do not meet the highest quality and safety standards present a risk of injury, recalls, embargos, bans and liability. The transition from IEC 60601-1 2nd Edition to the 3rd introduced the concept and application… read more

March 3rd, 2015
Designing for Compliance to IEC 60601-1 3rd Edition Workshop

Click here to register Description The medical device industry is the most heavily regulated in manufacturing, for good reason. Devices that do not meet the highest quality and safety standards present a risk of injury, recalls, embargos, bans and liability. The transition from IEC 60601-1 2nd Edition to the 3rd introduced the concept and application… read more

March 3rd, 2015
Designing for Compliance to IEC 60601-1 3rd Edition Workshop

Click here to register Description The medical device industry is the most heavily regulated in manufacturing, for good reason. Devices that do not meet the highest quality and safety standards present a risk of injury, recalls, embargos, bans and liability. The transition from IEC 60601-1 2nd Edition to the 3rd introduced the concept and application… read more

May 27th, 2014
EU Requires 60601 with Amendment 1 after 12/31/17

On May 16, 2014 the EU updated the Official Journal for the Medical Device Directive.  One of the updates was to include the EN versions of 60601-1 with Amendment 1.  After 12/31/2017, customers using the 60601-1 standard as a presumption of conformity will need to use the EN 60601-1:2006/A1:2013. For more information on the EU… read more