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UDI compliance deadline approaching

By aisltd Wednesday, 8th June 2016 | 0 comments
Filed under: Industry News.
With a deadline approaching in September 2016 for compliance with Unique Device Identifier (UDI) regulations, we in conjunction with our partner Microscan have put together some useful information on what exactly is involved.

EU FMD - Preparing for Compliance

By aisltd Monday, 30th May 2016 | 0 comments
Filed under: Industry News.
With the publication of the Delegated Act on safety features, those who manufacture, sell, or dispense medications in the European Union (EU) have until February 2019 to comply with complex new track-and-trace regulations outlined in the Falsified Medicines Directive (FMD).

UDI (Unique Device Identifier) Update

By aisltd Monday, 4th May 2015 | 0 comments
Filed under: Industry News.
The UDI system, which will be phased in over several years, offers a number of benefits that will be more fully realised with the adoption and integration of UDIs into the health care delivery system. UDI implementation will improve patient safety, modernise device postmarket surveillance, and facilitate medical device innovation.

EU Falsified Medicines Directive

By aisltd Monday, 2nd February 2015 | 0 comments
Filed under: Industry News.
Over the past few months it has emerged that the original compliance deadline of January 2016 has been pushed back to 2018. Wrestling with the technical and logistical challenges of implementation, those on the production floor could be forgiven for losing sight of the bigger picture, which is the need to safeguard patients and consumers against the danger posed by illicit medicines.