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Greenlight Guru Announces the Formation of Its New Regulatory Advisory Board
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Leading medical device QMS provider establishes Regulatory Advisory Board comprised of global regulatory experts
Greenlight Guru is continuing to push the ideal of harmonization and industry best practices forward through the formation of our Regulatory Advisory Board. INDIANAPOLIS (PRWEB) May 27, 2021 Greenlight Guru, the leading medical device quality management software platform, today announced the formation of its new Regulatory Advisory Board (RAB), comprised of nine veteran medical device professionals. Members of Greenlight Guru’s RAB have prior experience with regulatory bodies, including FDA and EU notified bodies, and have significant medical device industry expertise with respect to regulations, standards, and requirements impacting the medical device industry.
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