Quality and excellence that set standards
At SAS hagmann, quality and excellence are at the heart of everything we do. Our state-of-the-art facilities are equipped with the latest analytical tools and technologies to ensure we can deliver accurate and reliable data to our clients.
Our quality management: your guarantee of competence
The quality management system of SAS hagmann is geared towards the consistently high quality of our services.
Our accreditation according to DIN EN ISO 17025:2018, the recognition by the Central Office of the States for Health Protection with regard to Medicinal Products and Medical Devices (ZLG) and the confirmation of Good Manufacturing Practice (GMP) by the Tübingen Regional Council are evidence of our success and our commitment to the highest standards.
Accreditation
SAS hagmann GmbH & Co. KG is accredited by DAkkS, the only German accreditation body, according to the world’s highest quality standard for analytical laboratories.
Our unlimited accreditation certificate according to DIN EN ISO 17025:2018 and the successful extension audits, including the inclusion of additional methods such as ICP-MS and liquid chromatography, underline our competence and reliability.
Our accreditation certificates
ZLG recognition
SAS hagmann GmbH & Co. KG is recognized by the ZLG to test medical devices. This recognition reflects our ability to meet the high requirements for independence and impartiality in the field of medical devices.
Our expertise is also recognized internationally, as regulated by the agreement with the European Community.
The recognition of these competencies by the USA is regulated in an agreement with the European Community (OJ L 31 of 4 Feb 1999; Agreement Section 7. Medical devices).
The surveillance audit to confirm the recognized area was completed in May 2023 without deviations.
GMP confirmation
SAS hagmann GmbH & Co. KG has received confirmation of Good Manufacturing Practice (GMP) from the Tübingen Regional Council. This recognition demonstrates our strict adherence to the highest quality standards in drug monitoring, an area that is regulated in Germany by the respective regional councils.
Our GMP competencies, internationally recognized by the agreement with the European Community (OJ L 31 of February 4, 1999; GMP section), underline our commitment to quality and safety. The last routine inspection in March 2022 confirmed our consistent compliance with GMP standards, a testament to our commitment to excellence in drug manufacturing and safety.
About SAS hagmann: Your partner for quality and reliability
At SAS hagmann, the quality of our analytical services is our top priority.
We are proud to be an independent, family-run contract laboratory with decades of experience and in-depth expertise.
Our commitment to quality, coupled with state-of-the-art analytical methods and a strict quality management system, makes us a reliable partner for a wide range of industries.
Every question is the first step towards a new solution.
We are just a click away to answer your questions and provide you with our expertise. Fill out the contact form, and a member of our team will promptly get in touch with you. At SAS Hagmann, we are ready to listen and collaborate on solutions that truly make a difference.
