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Industry resource guides healthcare suppliers, providers

4/22/2014

GS1 Healthcare US releases implementation guideline for using GS1 standards to address FDA unique device identification (UDI).

Helping med device manufacturers meet UDI compliance

4/17/2014

Kallik’s AMS360 software is proving vital for medical devices firms who need to meet critical compliance directives.

Plan now to comply by 2016

4/10/2014

European medical device manufacturers face new regulations starting In 2016.

Resource for medical device manufacturing software validation

3/3/2014

InstantGMP’s web site resource assists new medical device manufacturers in understanding the requirements for software validation.

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