Episodes featuring Karandeep
About Karandeep's appearance on the show
Karandeep Singh Badwal, Founder, QR Medical & Host of The MedTech Podcast at QR Medical, 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 Karandeep - reach the next team that has to figure it out for the first time. If you're researching Karandeep Singh Badwal 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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Karandeep Singh Badwal is Founder, QR Medical & Host of The MedTech Podcast at QR Medical. Karandeep Singh Badwal is the founder of QR Medical, a quality and regulatory consultancy in the medical devices space. He also hosts The MedTech Podcast, where he interviews leaders and experts in the field.
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Karandeep Singh Badwal appears on 1 episode of The Med Device Cyber Podcast: Episode 9 - "Balancing Innovation and Regulation in MedTech Development with Karandeep Singh Badwal | Ep. 35".
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Across Karandeep's appearances, recurring topics include medical device, regulatory affairs, quality management system, samd, and ai in healthcare. These conversations focus on practical medical device cybersecurity guidance for MedTech teams.
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Quality management should be viewed as a proactive, preventative "defense" and a company-wide culture, while regulatory affairs is the "offense" focused on achieving market approval.
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