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 E-Mail The carbon footprint of plastic production for initial use is greater than the global warming impact of the entire process used for medical device reprocessing Use of reprocessed devices is environmentally superior to use of original products in 13 of 16 categories evaluated Reprocessing found to advance "circular economy," a key strategy for reaching the UN Sustainability Goals LCA offers evidence showing that in order to reduce greenhouse gas emissions and honor the Paris Climate Agreement, EU Member States must opt-in to EU Medical Device Regulation (MDR)'s reprocessing/remanufac...

Voice Prosthesis Devices And Equipment Market 2021 Global Industry Analysis, Opportunities, Size, Trends, Growth and Forecast 2030

Search jobs What Brexit and Covid-19 have revealed about supply chain efficiency Summary Covid-19 has tested supply chains across all sectors to their limit. For the European medtech supply chain – responsible for employing around 730 000 people – the pandemic has revealed that key lessons need to be learnt in order to maintain a consistent supply of equipment during turbulent times whilst also managing expenditure. A new report released by European MedTech supplier Healthcare 21 Group (HC21), sheds light on how healthcare businesses ca...

December 15, 2020 - CA US Compliance4All Phone:8004479407 Overview: This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU. It includes specific insights from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Areas of change between the prior Medical Device Directive (MDD) and the MDR will be discussed as well as expectations for how to implement ISO-13485:20...

Share it BRUSSELS — The European Commission this month launched the first component of its behind-schedule IT system for registering certified medical devices under looming new rules, but a regulatory bottleneck could render many products impossible to certify for some time.   The first of six modules of its Eudamed system will assign a "single registration number" to each medical device manufacturer, producer of procedure kits, importer, as well as the European representatives that non-EU manufacturers must have to get certified.    The database is incomplete and its roll-out two year...