Quality Management

The objective and purpose of our QM system is consistently high quality. Internal and external audits form a major integral part of accreditation to DIN EN ISO 17025.

The Zentralstelle der Länder für Gesundheitsschutz bei Arzneimitteln und Medizinprodukten (ZLG: Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices) recognizes SAS hagmann GmbH in accordance with Section 15, Paragraph 5, of the Federal German Medical Devices Act as a testing laboratory for medical devices as defined by Directive 93/42/EEC and 90/385/EEC as well as DIN EN ISO/EC 17025.

On request, an external audit appointment can be arranged at any time with our QMO
Our quality management system is based on written standard operating procedures (SOPs) that define all procedures relevant to quality. All audits are conducted in an independent, free, conscientious and unbiased manner. The traceability of all data, the proper storage of retention samples and the confidential handling of customer data are a matter of course for us.
The audit reports and expert assessments meet the requirements of DIN EN ISO 17025.

Accreditation for physicochemical and chemical investigations
Accreditation for medical products/devices
ZLG notification and scope of validity
ZLG recognition