A Regulatory Puzzle: Writing for the Medical Device Industry | Document360 Webinar

The world of medical device documentation—especially Instructions for Use (IFUs)—can often feel like solving a complex puzzle.

In this insightful session, Holly Mickelson, Senior Technical Writer at Brainlab, reveals how regulatory frameworks shape IFUs and how writers can turn those challenges into opportunities for clarity, consistency, and compliance.

Key Highlights:
►Regulatory impact: How global standards and notified bodies influence IFUs.
►Compliance vs. usability: Making IFUs both compliant and user-friendly.
►Hidden opportunities: Turning regulatory hurdles into better workflows and content quality.
►Actionable takeaways: Practical tips for writing clear, consistent, and compliant IFUs that build user trust.

𝐏𝐏𝐓 𝐒𝐥𝐢𝐝𝐞𝐬: https://bit.ly/3WvgWRK

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