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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
    • Courses
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    • Regulatory Accelerator
    • Startup Office Hours
    • Free Resources
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  2. Category "Seminars"

Seminars


Medical Devices – An Introduction to Product and Company Development in a Regulated Environment

By Anne Arndt16 June 2025Leave a comment

Discover how to successfully bring a medical device to market in this comprehensive 2-day introductory course. Two separate 2-day workshops are on offer for the second half of 2025. Dates: 23…

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qmsr

Top-Up Training: 21 CFR Part 820 – Preparing for QMSR

By Anne Arndt17 March 2025Leave a comment

Date: 15 & 16 July 2025 | Time: 1:00 PM – 5:00 PM NZT (Half-Day Sessions) | Price: NZD 800 | Place: Online via Zoom Prepare for the transition to the…

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PRRC Person Responsible for Regulatory Compliance Seminar

Seminar PRRC – Person Responsible for Regulatory Compliance – Nov 23-24

By Anne Arndt21 September 2023Leave a comment

Are you prepared for the crucial role of Person Responsible for Regulatory Compliance (PRRC) as required under EU’s MDR (2017/745) and IVDR (2017/746)? Is your organization in compliance with Article…

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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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