MIES has extensive experience in designing solutions for all types of applications, especially in the pharmaceutical industry and medical device sector.

In these industries, standards established for the production of sterile products are continuously becoming higher and require the manufacturer to be able to document the repeatability of the cycles and the full control of the equipment and its functions, that is, validate its processes.

On the other hand, the tendency towards parametrically releasing the manufactured batch to avoid quarantine at the end of terminal sterilization, results in these standards no longer being seen as an obligation but rather as a source of competitive advantage for the manufacturer.