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Hohenstein celebrated the opening of a second testing laboratory in Gurugram, India. The new addition to Hohenstein’s expanding lab network will focus on physical, colorfastness and restricted substance testing of leather, footwear and personal protective equipment (PPE).
In its 30th year of dedication to safer textiles and leather, OEKO-TEX® has created a new brand identity for higher recognition and more flexible labeling options.
The OEKO-TEX® RESPONSIBLE BUSINESS tool and certification will support brands, retailers and traders in the textile and leather sector with due diligence compliance. Due diligence requires companies to take legal responsibility for all human rights and environmental violations in their global supply…
With 30 years of experience, OEKO-TEX® offers standardized solutions that enable companies to optimize their manufacturing processes and help bring high-quality, sustainable products to market.
Hohenstein has extended its accreditations as a testing laboratory and certification body for FFP masks according to DIN EN 149.
Cloud-based data management platform, Texbase, announces collaboration with the global textile testing partner, Hohenstein. As a Texbase Lab Connect partner, Hohenstein customers can collaborate, send test requests and receive test reports within Texbase Connect.
Hohenstein has established a quality label for tested pet supplies to ensure product safety, quality and durability of pet blankets, beds, toys and other products.
Hohenstein is on the DLR's WICO2 team creating sensor-integrated garments to record & transmit physiological data from astronauts to Earth. The technology will be applicable to sports and medical applications.
Hohenstein developed a new quantification method specifically for genetically modified cotton. One of the first labs with this ability, Hohenstein uses DNA analysis to identify known genetic modifications and calculate their percentage in organic cotton.
The new EU Medical Device Regulation (MDR) comes into effect after a four-year transition period on May 26, 2021. The MDR replaces the Medical Devices Directive (93/42/EEC) and the Active Implantable Medical Devices Directive (90/385/EEC). Many Hohenstein test methods form the foundation for…