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27 Feb 2018 Defining a Family of Products to Economise Your Package Testing

By Noel Gibbons, Anecto Lead Programme Manager
Does every medical device’s packaging system need to be tested separately?
Most of the medical device manufacturers Anecto works with have straightforward packing testing needs. Usually they have a single product they wish to bring to market, and its product and packaging system need to be validated. In this case, […]

27 Feb 2018 The MDR: A Sign of Success

An Anecto opinion piece.
If you’re a medical device manufacturer, the persistent elephant in your room is probably regulation. This issue is best currently represented by the EU medical device regulations (MDR), which replaced the medical device directive (MDD) when published in May 2017, and is currently in a transition period.
In 2020, the MDR will be […]