Countdown to the Medical Device Regulation – A LANSA Perspective The changes happening in the medical device world over the next few years fall squarely into the category of “quiet revolutions that will affect us all.” The last time the European Commission updated and harmonised regulation across Medical Devices was in the 1990s – the … …
Continue readingGS1 UK Healthcare Conference 2015
LANSA was once again proud to be supporting GS1 UK at their annual Healthcare Conference in Holywell Park, Loughborough University on the 9th and 10th of June. As with last year’s event, LANSA was a Silver sponsor. We made the most of the two-day conference in terms of networking and promoting our newest PIM offering … …
Continue readingDQSA, FMD, Serialisation – Even more need for a Master Data Management (MDM) strategy, with a GS1 Compliant PIM at the heart
It’s a wonder we ever meet in person. With the explosion in digital technology we could just gather on Skype. The ease and convenience of online meetings oftentimes overshadows and underrates the value of actually getting together. This was amply demonstrated at the offices of Lifestar who recently hosted a meeting for the QP Forum. The Forum, … …
Continue readingBeyond Compliance and the FDA Unique Device Identification Rule – How to Achieve Global Standardization
As companies are faced with the challenges of managing Health Care information and are being required to comply with regulations in regional markets, many are asking: “Do we focus on regulatory compliance alone or is there a greater focus?” If regulatory requirements can be met at the same time as business initiatives to reduce costs, … …
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