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Die Stabilität und Haltbarkeit von Medizinprodukten ist entscheidend für Patientensicherheit, Produktzulassung und regulatorische Konformität. Doch wie prüft man die Haltbarkeit realistisch – ohne jahrelange Wartezeiten?

How can sustainability, patient safety, and regulatory requirements be combined in medical technology?

Various durability tests are used to determine in an accelerated form how a material, e.g. plastics, reacts to external influences…

The bubble test according to ASTM F2096, also called the bubble emission test or underwater leak test, is a qualitative, destructive method for…

Does your product need approval for shipping in its original packaging? We test your packaging material on calibrated test benches, document...

Explanation of IP rating with protection digits, meaning of foreign object and moisture protection in technical products.

The peel test is a central examination in packaging technology, especially in the medical technology, pharmaceutical, and food industries.

EU Packaging Regulation PPWR explains new EU requirements for packaging waste, recycling quotas, and sustainable design for manufacturers and retailers starting from...

The DIN EN ISO 17025 standard specifies the requirements for the competence, impartiality, and quality systems of testing and calibration laboratories on an international level…