The Dialog starts: Does medical technology need new concepts for validating cleanliness?

The aspect of cleanliness is deeply rooted in medical technology and regulations have been in existence for many years now. Despite this, problems due to inadequate product cleanliness still occur. There are also issues related to manufacturing technology where excessive cleanliness requirements are sometimes made. In this field of conflict, the following question arises: how to achieve a compromise on limiting values that ensures maximum patient safety but also allows meaningful and reliable results to be attained in production using validated test procedures?

Topics
•    Threshold validation versus practical cleanliness limiting values
•    Technical discussion with you as an expert

Goal
To initiate a dialog about new, practice-orientated procedures for assuring the quality of product cleanliness

Target Group
People from the entire supply chain of medical products who are responsible for quality, cleanliness, analytics and certification

Contact
Fraunhofer Institute for Manufacturing
Engineering and Automation IPA
Dr. Markus Rochowicz
Nobelstr. 12 | 70569 Stuttgart | Germany

Venue (Workshop Language is German)
Fraunhofer Institute for Manufacturing
Engineering and Automation IPA
Nobelstrasse 12, 70569 Stuttgart, Germany
Lecture Theaters A+B

Registration
To register for the event, please use the link stated below.

Survey on the topic of validating cleanliness in medical technology
www.ipa.fraunhofer.de/medizintechnik