TÜV SÜD Product Service, a Notified Body for Medical Devices, has issued a comprehensive EU quality management system certificate (IVDR) in less than four months.
CertifHy phase III will implement a harmonized H2 Guarantee of Origin (GO) scheme across Europe & beyond, build a market for H2 GO trade in close collaboration with market actors, and design a Certification Scheme for compliance with RED II renewable fuels for transport.
Like in previous years, TÜV SÜD Division Mobility supports medical projects with Christmas cards. In total, 10,000 Euros were collected during this charity campaign.
Simon Kellerer (39) will be appointed to the three-member management team of TÜV SÜD Industrie Service GmbH with effect from 1 January 2021.
TÜV SÜD recently launched a vegan product certification for apparel, footwear, and home textiles.
Software used for medical intended use is regarded as a medical device under the new regulation, a fact that is overlooked time and again by developers, manufacturers and distributors.
TÜV SÜD will participate in the 10th Aviation Forum, presenting extensive services in fields including additive manufacturing (AM), certification, environmental and non-destructive testing (NDT).
TÜV SÜD Product Service has issued their first In Vitro Medical Device Regulation (IVDR) certificate since receiving notification in June 2020 – and the first IVDR certificate worldwide.
The “new normal” is forcing companies to reconsider their existing plans, structures and processes and to seek out new solutions, including in cybersecurity.
On the occasion of World Standards Day on 14 October 2020, TÜV SÜD highlights international standards as being critical for the protection of our planet.
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