Our many years of know-how and modern equipment form the basis for good quality results, speed and reliability. In order to meet our quality standards, all employees regularly take part in training, further education and the exchange of experiences. Which goals can we support you with?
The requirements for medical devices in terms of risk management, purity and biocompatibility have increased continuously in recent years. We are happy to support you with regard to regulatory obligations (EU-MDR) and normative requirements (DIN EN ISO 10993).
We have been accompanying the automotive industry for decades, for example with residual dirt analyses (according to VDA 19) or in determining the residual amount of flux in aluminium-based heat exchangers. Our expertise in method development helps you meet the challenges of new technical specifications.
Whether material characterization at goods receipt, accompanying analyses in development or ause research in the event of damage, SAS Hagmann is a reliable and competent partner thanks to its many years of experience in a wide variety of industries.
The residue analysis of auxiliary and operating materials from chipping processing is not new territory for us, nor are salts from etching or pickling processes, electropolishing or passivation. Through constant contact with a wide variety of manufacturers, we can use our understanding to your advantage.
Both the characterization of the main polymer components and the detailed recording of additives and fillers are on of our core topics. UV stabilizers, flame retardants and glass fiber content are just as important to us as aging or leaching processes.
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