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The firm was ordered to identify the affected devices and contact the manufacturer to obtain a service kit or schedule machines for upgrade, prioritizing devices used at home. Read More
“Following recent market developments, we have made the strategic business decision to exit from [notified body certification] services,” said Lloyd’s Register Quality Assurance. Read More
With less than one year before the EU’s Medical Device Regulation takes effect, an industry group is raising increasing alarm about the lack of “essential guidance” and the shortage of notified bodies needed to certify products in compliance with the new requirements. Read More