05.07.2019
The introduction of digitalisation for lifts poses a challenge for lift and component manufacturers to ensure not only functional safety but also IT security. At interlift 2019, which will take place in Augsburg from 15 to 18 October 2019, TÜV SÜD will present its comprehensive range of services for ensuring the safety and security of smart lifts. (Hall 5, Stand 5.033)
25.06.2019
作為賽事唯一的白金贊助商，全球知名的第三方認證檢測機構TÜV南德意志集團受邀出席了本次比賽，鼓勵青年學生勇于創新，共同推進香港科技發展。
20.06.2019
TÜV南德意志集團面向現場的來賓介紹了TÜV南德在LED照明產品領域的測試認證服務，并攜手中國標準化研究院舉辦“LED照明產品能效國家標準宣貫會”。
12.06.2019
2020年5月26日，歐盟醫療器械革命性法規MDR（Medical Device Regulation）將全面強制執行，TÜV南德大中華區醫療健康服務副總裁陳昭惠接受了《進出口經理人》采訪，表達了她的觀點。
03.06.2019
ANSF, Italy's National Railways Safety Agency, has recognised TÜV Italia as Verificatore Indipendente Sicurezza (VIS). Based on this recognition, the inspection and certification organisation can now provide assessment of railway systems according to Italy's Notified National Technical Rules (NNTR-I). TÜV Italia is a 100% subsidiary of the TÜV SÜD Group and supplies all its rail services under the umbrella of the Rail business unit.
29.05.2019
Gerhard Müller (56), Head of Public Policy and Economic Affairs of the Mobility Division of TÜV SÜD, was elected new President of the Comité International de L’Inspection Technique Automobile (CITA) by the CITA General Assembly in Seoul, South Korea, in April 2019. This is the first time that a TÜV SÜD employee has headed the International Motor Vehicle Inspection Committee, which has 135 members representing over 50 countries. The key topics for Müller’s four years of presidency concern advancing international road safety, establishing global standards for the testing of automated driving functions and further reducing vehicle emissions.
23.05.2019
TÜV SÜD Product Service is among the world's first certification bodies to receive designation as a Notified Body for the new Medical Device Regulation (MDR) by the Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG). The European Parliament implemented the MDR to improve the EU approval system for medical devices. The regulation which came into force in May 2017, will end its transition period by late May 2020.
23.05.2019
Even one year after the end of the transitional period, German companies still have a lot to do to fully meet the requirements of the General Data Protection Regulation (GDPR). According to a recent survey by TÜV SÜD, around one third of those surveyed said that their company had implemented the necessary measures only partially (29%) or not at all (6%).
23.05.2019
The quality of metal powder is a crucial factor for reliable additive manufacturing (AM) using laser powder-bed fusion (LPBF) machines. TÜV SÜD Industrie Service GmbH has now completed its first audit of a manufacturer of metal powder at Rosswag GmbH. The audit forms part of a new certification programme based on the AD 2000 Code for pressure equipment and thus, mutatis mutandis, the European Pressure Equipment Directive (PED).
17.05.2019
Japanese experts from TÜV SÜD Japan, a member of one of the world’s leading technical service organizations, have completed their first project under INMETRO Ordinance No. 54/2016 governing medical devices. The organization issued an INMETRO certificate for active medical devices based on this INMETRO Ordinance on January 21, 2019. In the future, TÜV SÜD Japan will continue to support medical device manufacturers who need to transition to INMETRO Ordinance No. 54/2016 and medical device manufacturers who intend to sell medical devices in Brazil.
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