There is hardly any other sector that faces such complex requirements regarding product information and labelling as the pharmaceutical industry.
Due to continued expansion in the Munster region, we are excited to announce that we have just opened a new office in Eastgate Park, Little Island, Cork.
The ALTech machine of the month is an ALstep built for an important producer of plastic containers.
Materials produced in a continuous roll or sheet, such as paper, textiles, film, foil, plastics, metals, glass, or coatings, are best inspected by line scan systems.
Our customer, a global medical device company which manufactures filters for particle monitoring, needed to streamline their labelling process across 4 production lines.
We will be exhibiting at the 3rd National Food & Drink Business Conference and Exhibition on 14th of September in Citywest Convention Centre, Dublin.The theme of the event is Collaborating For An Innovative Food Island.
The recent edition of the Chambers Ireland publication features an article on the services offered by AIS Ltd (pg 82). View your copy here.
Our customer, an international medical devices company based in the West of Ireland, develops, manufactures, and markets healthcare products and services worldwide.
Verify Barcode presence, data and perform OCR (Optical Character Recognition) on text fields in one pass. Suitable for the Food & Beverage/Pharmaceutical Industry.
AIS are looking for 2 recent graduates that are ready to be challenged in a fast paced commercial environment. If you are highly motivated, a self-starter, interested in a career in sales and solution selling into the life sciences industry, this could be the role for you!
The next deadline in the FDA's Unique Device Identification (UDI) regulation will hit September 24, 2016 – and it's not just about your medical device packaging anymore! Register here.
We at AIS Ltd know labelling machines so if you have a requirement for an automatic label applicator, here are some things that you should consider when buying:
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.
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).
Our customer, a global medical device manufacturer, was tasked with automating their highly manual end of line packaging process.