IPP provides a range of equipment which is commonly used by blue-chip medical device companies in the final assembly and test areas of their manufacturing processes.
We offer a range of medical device pouch and tray sealers, non-destructive package test equipment, electronic label inspection and verification systems, industrial ovens for curing and device coating, and also equipment
Martindale has purchased 5 lines of Track and Trace Equipment at our site in Romford. The project is well underway, to date 3 lines are fully installed. We have been very satisfied with their performance as a partner and with the local management and support from IPP / Mettler Toledo
At Noumed we purchased 4 lines of Serialisation equipment from IPP / Mettler Toledo, we have 2 fully installed and the other two have completed FAT. We are very happy with the support we got from IPP Ltd during the project and the local support has been very good.
The European Medical Device Regulations were published by the European parliament in April 2017. Like the EU Directive on Pharmaceuticals which preceded them, it means that any company supplying Medical Devices in the European Union (even those manufactured outside the EU) are legally obliged to comply or they are breaking the law. Yes, it’s very black and white.
Medical Technology Ireland, 25 and 26 September 2019, Galway Racecourse, Stand 39.
Recent years have seen a significant rise in the use of pre-filled syringes (PFS) as a containment solution for pharmaceutical products. This trend is expected to accelerate over the coming decades. For the pharmaceutical company, the advantages of prefilled syringes are minimizing drug waste and increasing product life span.