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Almost Three-quarters of Medical Device Companies Ready to Meet the European Union s MDR and IVDR Regulations, According to RWS Research
05/10/2021 | 03:01am EDT
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Despite optimism, almost half admit COVID-19 will have long-term impact on strategic planning
A research report from RWS, the world’s leading provider of technology-enabled language, content management and intellectual property services, highlights the impact of COVID-19 on medical device manufacturers, and their readiness to meet the European Union’s (EU) Medical Device regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) deadline.
The research, involving leading medical device organizations operating in Europe, looks at how the pandemic has affected their preparations to meet the 26 May 2021 deadline for the EU MDR, and EU IVDR deadline of 26 May 2022. The research paints an optimistic picture: almost three-quarters (70%) of organizations are positive about meeting the MDR deadline,
Greenlight Guru Announces True Quality Summit Series: EU MDR & IVDR
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Leading MDQMS provider combines global regulatory leadership with original research data to provide the most comprehensive European regulatory event in the medical device industry.
The upcoming summit will pull together some of the brightest minds in the industry to share insight and tips to ensure compliance as we take on another year of change. INDIANAPOLIS (PRWEB) February 12, 2021 Greenlight Guru, the leading medical device quality management software (MDQMS) platform, today announced the True Quality Summit Series: EU MDR & IVDR, a free, five-day online event to help quality, regulatory and product development professionals understand the new EU medical device regulations and how companies can be both successful and competitive in the European market once MDR and IVDR go into effect. The True Quality Summit Series will take pl