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We will be exhibiting in Hall B6 at Stand 154 during the Wind Energy Hamburg show in Hamburg, Germany from 25th – 28th September.
If you wish to organise a meeting with one of our representatives, please…
Making Sense of the Latest Luer Requirements
By Philip Roxby, Programme Manager of Technology and Test Development
With the release of a new standard for Luer connectors, many medical device manufacturers are now striving to achieve compliance with both new and legacy connectors.
With that in mind, Anecto has prepared a short white paper outlining the most important […]
We will be exhibiting at a number of events in 2018.
Anecto will be exhibiting at Stand 75 during the Medical Technology Ireland show on 26th & 27th September at Galway Racecourse.
As part of the event, Anecto will also be hosting a Networking Drinks Reception in the Clayton Hotel, Galway on the evening of Wednesday 26th September […]
With the roll-out of Amazon’s Frustration-Free Packaging Programs, Anecto would like to remind any Amazon vendors that we are an ISTA-certified test laboratory and can fulfil your testing needs, including the ISTA 6-Amazon.com Ships in Own Container (SIOC) test procedure.
Amazon’s new program prioritizes packaging that reduces waste, is easy to open, is recyclable, and ultimately […]
IBEC’s ‘Polymer Technology Ireland 2020 Strategy’ features a business case study on Anecto and our role in supporting the Irish plastics industry.
Anecto Director of Testing Services, Michael Connolly, was interviewed for the piece, titled “The test of time.”
It focuses on Anecto’s development over the years, including the company’s varied testing capabilities, our test work with […]
By Phil Roxby
As a test laboratory for medical devices, our purpose is to help product developers along their journey toward regulatory compliance. Due to the all-consuming nature of designing a brand new product, developers are frequently more focused on functionality than risk.
This is perfectly normal considering the long process between conception and clinical trial. However, […]
ISTA recently made changes to its 3A test procedure with the addition of a leak test for packaged products which contain liquids. The purpose of the change, published in March, is to “evaluate the closure system’s ability to contain the liquid after all other 3A testing elements have been completed.”
The leakage test requires the product […]
Independent, award-winning and accredited test laboratory Anecto is excited to invite you to participate in an upcoming seminar on Medical Device packaging:
Date: Tues 5th & Wed 6th June, 2018
Venue: Hotel allgäu resort
87730 Bad Grönenbach,
What to Expect?
This 2-day educational seminar will include presentations, poster sessions, workshops and a plant tour that will all focus […]
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, […]
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 […]