Medfor is committed to the manufacture and supply of storage products and services which fully meet our customers' requirements first time, on time, every time, through a system of quality management affecting all aspects of the operation. This is achieved through training and ongoing assessment, and is the collective responsibility of all employees of the company.

Most of the parts used in assembling our products are manufactured from primary food grade plastic that has been produced under ISO 9001:2000 conditions. All product assembly is performed in a controlled environment that is subjected to positive pressure and monitored to keep the number of microbiological organisms and particles to a minimum.

The company is registered to ISO 9001:2000 and ISO 13485:2003, the latter containing additional requirements to meet medical device regulations. These standards, which are subject to regular audits by external experts, include complete batch traceability and the careful vetting of suppliers.

To download Medfor's quality certificates in PDF format, go to the Downloads section of our website.