Peabody, Massachusetts. TÜV SÜD America Inc. is pleased to announce that it will co-sponsor a luncheon at the QuEST Forum 2012 Americas Best Practices Conference. The luncheon will be on Wednesday, September 12, 2012 at 12:00 p.m. - 1:30 p.m.
Taking place on September 10-12 at the Chicago Oak Brook Hills Marriott Resort in Oak Brook, Illinois, the conference is an annual event for telecommunication technologies professionals. The conference offers networking opportunities and intensive learning experiences through a blend of panel discussions, keynote speakers, workshops, and executive sessions. Topics include the latest tools, techniques, and methodologies to help organizations achieve and sustain business excellence.
TÜV SÜD's Management Service division is accredited by the ANSI-ASQ National Accreditation Board (ANAB), to provide TL 9000 certification services. In addition, TÜV SÜD America offers thorough BABT Production Quality Certification (PQC) and BABT full-quality assurance (FQA) approval under the Radio & Telecommunications Terminal Equipment Directive (R&TTED).
For more information about the full suite of services available from TÜV SÜD America, visitwww.TUVamerica.com.
For more information, contact:
TL 9000 Program Manager
TÜV SÜD America Inc.
For editorial information, contact:
Marketing Communications Specialist
TÜV SÜD America Inc.
About TÜV SÜD America Inc.
TÜV SÜD America Inc., a subsidiary of TÜV SÜD AG, Munich, Germany, is a leading globally recognized testing and certification organization. TÜV SÜD's Auditing Division provides management system certification services to ISO 9001, ISO 14001, AS9100, ISO 13485, Safe Quality Food (SQF), and more. TÜV SÜD's Testing Division offers Electrical and Mechanical Product Safety, Electromagnetic Compatibility (EMC) testing, Environmental Testing, NRTL and SCC certification, CE Marking assistance, Restricted Substance Services, International Compliance Services, and more. TÜV SÜD America also provides a diverse suite of services as a European Union Notified Body for the In Vitro Diagnostic, Medical Device, and Active Implantable Medical Device Directives, along with CMDCAS services, FDA 510(k), and third-party inspections. The company's Industry Division offers a full suite of services for pressure equipment manufacturers and materials producers exporting products to the European Community.