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  • Services
    • Regulatory Consulting Services
    • SaMD Consulting Services
    • External PRRC
    • External QMR
    • In-Country Representation
    • Regulatory Monitoring
    • Micro Consulting
  • Training
    • Medical Device University
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    • Regulatory Accelerator
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11 July 2023


Free FDA Cybersecurity Webinar

Free Webinar: Unpacking the FDA’s New Cyber Security Legal Requirements for Medical Devices

By Anne Arndt11 July 2023Leave a comment

Do you need help understanding the new US Food and Drug Administration’s (FDA) legal requirements for cybersecurity in medical devices? We’ve got you covered. On August 17th at 11 a.m.…

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New Zealand Therapeutic Goods Bill

Revamping Regulation: The Imperative Shifts in New Zealand’s Therapeutic Products Bill

By Anne Arndt11 July 2023Leave a comment

The Therapeutic Products Bill, promising to revolutionize the regulatory landscape for therapeutic goods in New Zealand, has stirred intense discussions among experts and industry insiders. A recent event that vividly…

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