TUV Rheinland

TÜV Rheinland PTL, LLC, North America’s largest solar and photovoltaic testing company, was certified by the Solar Rating and Certification Corporation (SRCC) to perform solar thermal testing and performance verification.

The Standards Institution of Israel and TÜV Rheinland have reached a strategic cooperative agreement allowing TUV Rheinland to test and certify electrical products and components destined for the Israeli and global marketplace.

TÜVRheinland®, the worldwide leader in global market access, and the Washington State Department of Commerce are offering a half-day seminar about the amendments to the Medical Device Directive as a result of the new Directive 2007/47/EC.

Figures from 13 years of solar technology testing – including the top three quality failures and strongest influences on module design – show some photovoltaic (PV) modules required a tune-up to pass international qualification standards.

Poor-quality solar energy equipment could flood the U.S. market without the safeguard of third-party testing and certification. Newly announced recommendations by Solar America Board for Codes and Standards protect consumers and businesses alike.

TÜVRheinland releases its latest schedule for the International Approvals roundtable series: Global Regulatory Approval of Products. The event helps answer manufacturer questions about market access & the process for gaining international approvals.

TÜVRheinland has released a case study called “Product Safety: Compliance Testing and Certification” highlighting its efforts to help Moore Industries-International, Inc. certify its new STA Safety Trip Alarm to IEC 61508: Parts 1, 2 and 3.

TÜVRheinland, the leading provider of testing and certification services for global companies, is announcing its 2010 schedule for the International Approvals roundtable series: Global Regulatory Approval of Products in the United States.

Starting March 21, 2010, all medical device manufacturers must comply with the Directive 2007/47/EC or risk being pulled from the EC market. Manufacturers can learn more about the Medical Device Directive at a seminar hosted by TÜVRheinland.

Companies are facing unique challenges as they export products into emerging global markets. For those new to the export world, the Department of Commerce’s U.S. Commercial Service is offering a new seminar called “International Market Access”.