News & Events from the Medical Devices Sector
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.
March 11, 2021
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.
New product innovations in the medical device industry drive an ever-increasing demand for faster and more reliable leak testing. From legacy products such as catheters to the modern developments in pressurized wound dressings, the challenge always remains to find more efficient and reliable test methods in order to reduce cycle times while still maintaining reliability in the quality of the test method.
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Birmingham, UK, 5 February 2019: From 1 March 2019, UK based Anglo Production Processes (APP) Ltd and Irish limited company, Industrial Power Tools (IPT) Ltd will trade under one brand identity, Industrial Production Processes (IPP) Ltd.
This week PTI awarded IPT for its Outstanding Customer Support in 2018.
This week IPT became the Irish distributor of Super Dry® Totech. Super Dry® Totech began nearly a decade ago as a distribution and technical support channel for ultra-low humidity dry cabinets with patented Zeolite technology.
Medical Technology Ireland, 26 and 27 September 2018, Galway Racecourse, Stand 16.
IPT is now Accu-Seal’s official partner in Ireland.
Visit IPT’s stand G3 at the National Life Sciences & Engineering Expo, Mullingar, 28 and 29 June
The UK’s Medicines and Healthcare products Regulatory Agency issued a warning that sterility may be compromised in Ecolab’s Klerpack BD syringe multi-pack due to small holes in the packaging.
VeriPac inspection systems are deterministic test methods for package integrity testing that produce reliable and robust quantitative test data.
The European parliament finally published the delegated acts in February of this year, allowing producers 3 years to become compliant with the regulations. The addition of a unique code on the carton coupled with an anti-tamper device on the carton itself is a positive move by European Authorities to protect the consumer from counterfeit products entering the supply chain.
We’re only a few weeks into the new year and already I have a great feeling about what lies ahead. SencorpWhite is continuing its solid tradition of mixing old-fashioned customer service and know-how with cutting-edge solutions to keep our customers a step ahead of their competition.
The next generation of Medical Device Pouch sealing.
Planning to visit MedTech UK on 15 and 16 May 2019?
August 17, 2020
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