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  • Medical Devices

    Rigid regulatory obligations leave no room for error in the Medical Devices industry. Discover a range of articles and resources that highlight the importance of Standards to eliminate manual workflow processes, reduce risk and bring products to market safely and quickly.

  • All Resources

    MDR 2021?
    Standards Insights
    Understanding the medical device risk management Standard ISO 14971:2019
    3-min read
    Predictability in medical devices
    Whitepaper
    EU MDR transition and the implications on the MedDev industry
    8-min read
    MDR 2021?
    Standards Insights
    3 important Standards to control the spread of infection
    2-min read
    Predictability in medical devices
    Industry Insights
    Staying on top of MDR regulatory requirements past the transition date
    3-min read
    ISO 14971:2019
    Industry Insights
    The power of predictability within the MedDev industry
    4-min read
    MDR 2021?
    Standards Insights
    Quality management systems in Medical Devices with ISO 13485
    4-min read
    Predictability in medical devices
    Industry Insights
    Top 4 medical device advancements and the future of MedDev
    3-min read
    MDR 2021?
    Industry Insights
    Medical device labelling requirements and related Standards
    3-min read
    Predictability in medical devices
    Standards Insights
    Essential international Standards guiding critical practices within the MedDev industry
    3-min read
    ISO 14971:2019
    Industry Insights
    Securing healthcare records and privacy in Australia
    3-min read
    MDR 2021?
    Standards Management
    Gain instant access to critical Standards related to the entire device lifecycle
    3-min read
    Predictability in medical devices
    Industry Insights
    Keeping up with quality requirements past the MDR transition
    3-min read
    MDR 2021?
    Key Standards
    Standards play an important role in meeting safety, quality and efficiency requirements
    3-min read
    Predictability in medical devices
    Industry Insights
    MDR 2021? Understanding the delay of EU MDR 2020
    3-min read
    ISO 14971:2019
    Mini Guide
    Guiding healthcare providers on sterilising techniques
    3-min read
    MDR 2021?
    Industry Insights
    Is EU MDR 2020 the Brexit of the Medical Device industry?
    3-min read
    Predictability in medical devices
    Industry Insights
    The implications of MDR requirements to product development
    3-min read