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Learn how to meet new EU Medical Device Regulation requirements to maintain market access, and certify in-scope products before the deadline.
Join Assent’s EU MDR experts as they explain what the EU MDR means for companies and what steps can be taken to bring older devices into compliance.
Join Bruce Jarnot as he discusses how to update your compliance program to collect new product information and meet the TSCA deadlines.
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The Act for Resource Recycling of Electrical and Electronic Equipment and Vehicles (commonly known as Korea RoHS) was adopted by the National Assembly of Korea on April 2, 2007 and entered into force on July 1, 2008. Read More...