MEDICAL PLASTIC COLOUR COMPOUNDING

     Matrix Medical Plastics operates from a fully compliant site. Process control is of paramount importance in the medical sector, so we ensure that all aspects of our production process satisfy the most stringent of quality requirements.

     All medical products are processed and tested according to ISO Class 9 cleanroom regulations and under ISO 13485 quality management systems for medical devices.

     All ingredients used on site in the production of medical products meet the requirements of ISO 10993-1:2018 and USP Class VI.

     Matrix Medical Plastics operates in a medical environment facility with dedicated processes and operations to comply with the precise requirements of the medical industry.

     We pride ourselves on being the UK's first 'cleanroom' plastic compounding facility with a sterile manufacturing environment and impeccable hygiene standards.

     Our strictly controlled manufacturing facility and high-quality ingredients ensure that all products are produced in accordance with WHO and FDA Good Manufacturing Practices.

     Matrix Medical Plastics has the expertise and experience to facilitate full regulatory support documentation and change control for up to 3 years to ensure consistent quality for every customer.

     We work closely with customers and suppliers to maintain high levels of transparency around quality and compliance; our commitment to process control is unparalleled.

     Additionally, full laboratory testing is available covering a comprehensive range of microbiological and chemical testing at any point of the manufacturing process.