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Testing and certification of lifts and their components

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)

鼓励科技创新,TÜV南德赞助出席香港机械人大赛

25.06.2019

作为赛事唯一的白金赞助商,全球知名的第三方认证检测机构TÜV南德意志集团受邀出席了本次比赛,鼓励青年学生勇于创新,共同推进香港科技发展。

TÜV南德携手中标院举办LED照明产品能效国家标准宣贯会

20.06.2019

TÜV南德意志集团面向现场的来宾介绍了TÜV南德在LED照明产品领域的测试认证服务,并携手中国标准化研究院举办“LED照明产品能效国家标准宣贯会”。

陈昭惠:价值驱动,迎接MDR时代的到来

12.06.2019

2020年5月26日,欧盟医疗器械革命性法规MDR(Medical Device Regulation)将全面强制执行,TÜV南德大中华区医疗健康服务副总裁陈昭惠接受了《进出口经理人》采访,表达了她的观点。

TÜV SÜD assesses rail systems in Italy

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.

TÜV SÜD: Gerhard Müller elected CITA President

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.

TÜV SÜD certifies Rosswag as manufacturer of metal powder for additive manufacturing

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).

Survey: Still great need for action regarding GDPR

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%).

TUV SUD becomes second Notified Body receiving designation

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.

First active medical device project completed by TÜV SÜD Japan

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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