News & insights
Company updates, capability investment, quality certification, regulatory commentary and technical notes on silicone applications.
A practical walk-through of the liquid silicone rubber (LSR) moulding process — from material chemistry and tool design to cure kinetics, cleanroom integration and validation — written for design engineers specifying silicone components for regulated markets.
EU MDR transition deadlines, the UK's post-Brexit medical devices framework and updated biocompatibility expectations under ISO 10993 are reshaping how silicone components are specified and evidenced.
Our quality management system has been recertified to ISO 13485:2016 by LRQA following a successful reassessment audit. The new certificate runs to 29 March 2029.
Durometer, extractables, cure system and secondary operations all shape whether a liquid silicone rubber is the right choice for a drug-delivery seal, valve or reservoir component.
ISO 14644 classification is only part of the story. Gowning, airflow, particle monitoring and how the moulding process itself is set up all decide whether an ISO 8 cell delivers on its promise.
A new MAPLAN 160-tonne vertical injection moulding machine has been delivered and commissioned at our cleanroom facility, adding dedicated LSR capacity for medical and drug-delivery programmes.
