Check out our latest seminars held across Asia Pacific and how our customers have benefited from them, as well as highlights of our recent certificate awards ceremony.
Awareness of ISO/ TS 16949:2009, Indonesia
ISO/TS 16949:2009, in conjunction with ISO 9001:2008, defines the quality management system requirements for the design and development, production and, when relevant, installation and service of automotive-related products. TÜV Rheinland Indonesia supported companies in the automotive industry with a seminar “Awareness of ISO/TS 16949:2009” in March 2016. Nearly 40 participants attended to understand the elements of ISO/TS 16949:2009 standard.
REACH Regulation Compliance - Sustainable Development, Vietnam
With state-of-the-art equipment, TÜV Rheinland Vietnam’s Softlines laboratory brings one-stop services for manufacturers and buyers around the world in accordance with national and international standards. As an added value service, TÜV Rheinland Vietnam conducted a seminar “REACH Regulation Compliance - Sustainable Development” in March 2016 for existing and prospect clients.
The participants learned about chemical management in context, the basics of REACH Regulation, Substances of Very High Concern in the Candidate List, and REACH Restriction List.
Series of Seminars: Introduction of ISO 45001, Japan
OHSMS (Occupational Health and Safety Management Systems) ISO 45001 will be issued around October 2016, and in conjunction with this, TÜV Rheinland Japan held an introduction seminar in Yokohama, Osaka, Hamamatsu, and Fukuoka to explain:
• History of OHSMS
• Effect of the system implementation (benefit of industrial injury insurance)
• Introduction to ISO 45001
• Difference between OHSAS 18001 and ISO 45001
The implementation of OHSMS helps to safeguard employees’ safety, more efficient operation and in winning customers’ trust.
Series of Seminars: Medical Equipment Installed Software – Japan/US/EU Regulatory Compliance, Japan
TÜV Rheinland Japan is holding a medical series “Medical Equipment Installed Software – Japan/US/EU Regulatory Compliance” from 2015 to 2016.
In this seminar, explanations are provided for general requirements, EU harmonized standards, FDA guidance, and international standards for manufacturing / distribution of medical equipment installed software in Japan/US/EU. Related standards are also introduced:
• IEC 62304 Medical Device Software - Software life cycle processes
• FDA Guidance (US Food and Drug Administration)
• IEC 62366 (Medical Devices - Application of usability engineering to medical devices)
• ISO 14971 (Medical Devices -- Application of risk management to medical devices)
• ISO 13485 (Medical Devices -- Quality management systems -- Requirements for regulatory purposes)
Certificate Awards Ceremony
PT Aplikanusa Lintasarta Certificate Awards Ceremony
Date: 18 March 2016
Name of Organization: PT Aplikanusa Lintasarta
Scope: Corporate Solutions: Data Communications, Internet and IT Services
About the Organization: Established in April 1988, Lintasarta is a leading company in information and communication technology services. Lintasarta serves more than 1,700 partner companies and are connected to more than 20,000 networks, with local support in more than 44 cities across Indonesia.
E Ganzon, Inc. Certificate Awards Ceremony
Date: 13 April 2016
Name of Organization: E Ganzon, Inc.
Standard: ISO 9001:2008
Scope: General Construction: Development, Selling and Leasing of Real Estate
About the Organization: E. Ganzon, Inc. was registered in October 1982 as a construction services company. It offers the whole gamut of general building and general engineering services such as civil works, structural, plumbing and sanitary, electrical, mechanical and other specialty works.
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