Innovative design, highest standards of quality control, 10 cleanrooms & ISO 13485:2016 accreditations
Designed with the aim of manufacturing innovative packaging and medical devices to improve common medical procedures. The state of the art 4,700 sq metre medical device manufacturing facility has been tailor-made specifically for the manufacture and packaging of medical products. It houses 8 Cleanrooms (two Class 8 and six Class 7), each being either product or process specific.
We process some of the most advanced medical packaging materials available in the industry. Pouches and sachets are regularly checked on-line for conformance to specification and seal integrity. Off-line seal strength, burst and die penetration testing is routinely carried out on pouches, sachets and blisters in accordance with EN 868 Part 1.
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ISO 13485:2016 | JPAL | CE 01865 |