Greenlight Guru's State of Medical Device Product Development and Quality Management 2020 Report is here.
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ISO 13485:2016 Changes You Should Know About
The bottom line? YOU ONLY HAVE UNTIL 2019. Knowing what is changing and making plans to comply early will save your company hassle down the line and possible issues with non-compliance.
Learn more about ISO 13485:2016 in our article:
Key Challenges for Risk Management in Medical Device Development
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