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Our in-house AEMP continues to grow

Demand for our validation services in the field of VMP (validation of reprocessing for medical device manufacturers) is growing steadily. As a result, the decision was an easy one to further expand the equipment in our in-house medical device reprocessing unit and bring it up to the latest state of the art. This took place in June 2020 (see also News: New AEMP Building)

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And it continues…

…the next expansion is already underway after less than a year. The RDG-E from Steelco rounds out our capabilities and enables us to meet the numerous requests for the reprocessing of medical devices in accordance with DIN ISO 17664 even more efficiently. This state-of-the-art technology ensures optimal reprocessing while reducing water, chemical, and energy consumption. We look forward to the upcoming projects!

You can find more interesting topics on reprocessing validation for manufacturers here: MP-MANUFACTURERS

Your Partner for Quality, Safety, and Compliance

The life sciences sector requires specialized knowledge and reliable support. With our comprehensive expertise, we help companies comply with laws and regulations, ensure quality, and continue to innovate with confidence.

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