Episodes featuring Jim
About Jim's appearance on the show
Jim Goodmiller, Consultant at Bio Bridges, joined The Med Device Cyber Podcast to share field-tested perspective with our audience of medical device security engineers, regulatory leads, quality teams, and MedTech founders. Every guest we book has either personally led an FDA cybersecurity submission, shipped a connected device into clinical use, or worked the disclosure and remediation side of a real-world vulnerability - we don't run vendor pitches or keynote-style overviews.
The Med Device Cyber Podcast is produced by Blue Goat Cyber, a specialist medical device cybersecurity firm whose hosts have walked submissions through FDA, ISO 14971 risk management, IEC 62304 software lifecycle expectations, and SBOM hygiene under the Refuse-to-Accept policy. The show exists so the lessons learned by people doing this work daily - guests like Jim - reach the next team that has to figure it out for the first time. If you're researching Jim Goodmiller for a hiring decision, an advisory call, or to invite them onto your own programme, the episodes below are the most current public record of how they think about the problem.
Want to keep exploring? Browse all our guests, jump to the complete episode catalog, or check our FDA Premarket, Postmarket, and Threat Modeling topic hubs for related conversations.
Frequently Asked Questions
Quick answers drawn from this episode.
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Jim Goodmiller is Consultant at Bio Bridges. Jim Goodmiller has 30 years of consulting experience, with a background spanning IT and life sciences. He works with Bio Bridges to guide companies from concept to commercialization, offering strategic consulting solutions and resources on a fractional basis.
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Jim Goodmiller appears on 1 episode of The Med Device Cyber Podcast: Episode 36 - "How Cybersecurity Shapes Regulatory and Quality Success with Jim Goodmiller | Ep. 49".
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Across Jim's appearances, recurring topics include medical device cybersecurity, fda regulation, quality management, life sciences, and medtech startups. These conversations focus on practical medical device cybersecurity guidance for MedTech teams.
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Cybersecurity in the medical device industry is no longer just an IT issue; it is a critical component of regulatory and quality compliance.
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