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Watch practical medical-device cybersecurity webinars and find conferences where Medcrypt experts are speaking about regulatory readiness, secure design, and lifecycle risk.

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Cleared vs. Refused: What Recent FDA Reviews Reveal About Cybersecurity

FDA ComplianceFDA Cybersecurity Readiness

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Webinars are online sessions you can register for or watch on demand. Conferences are in-person industry events where Medcrypt experts are presenting, participating, or sponsoring.

Showing 1–9 of 61 events

November 16, 2026

Topics: FDA Compliance, +7 more

Cleared vs. Refused: What Recent FDA Reviews Reveal About Cybersecurity

What recent FDA reviews reveal about cybersecurity evidence, CVSS, and getting devices cleared

October 14, 2026

Topics: Risk Management, +1 more

Fixing the Threat Modeling Ownership Problem

Turn a once-and-done threat model into a living part of your security program.

September 23, 2026

Topics: Cybersecurity Leadership, +5 more

Find Your Gaps Now: Healthcare Cybersecurity Data for Your Next Submission, Roadmap, and Board

What five years of healthcare cybersecurity data means for your next submission, your roadmap, and your board.

September 17, 2026

Topics: Artificial Intelligence, +2 more

AI and Cybersecurity: Risks, Opportunities and Considerations for the Medical Device Industry

AI is reshaping medical device security — from both sides of the fight

June 17, 2026

Topics: EU MDR, +2 more

Compliance is the New Cost of Doing Business

Why medical device manufacturer C-suites are now on the hook for cybersecurity — and what the next 12 months will demand.

March 18, 2026

Topics: FDA Compliance, +3 more

The New FDA Inspection Reality: Navigating the Shift from QSIT to QMSR & Section 524B Cybersecurity Audits

Bridging the Gap Between Quality Management and Mandatory Cybersecurity

March 12, 2026

Topics: EU MDR, +3 more

Medical Device Cybersecurity - Changing Software Regulatory Environment in the EU for Manufacturers

Mastering MDR CRA, NIS2 and AI Act

February 4, 2026

Topics: FDA Compliance, +3 more

Mastering Postmarket Surveillance: Why and How

Master the complexities of FDA & MDR postmarket requirements with expert-led insights.

January 28, 2026

Topics: Cybersecurity Leadership, +5 more

Secure by Design or Deficiency by Default: Navigating the FDA’s 2026 Inspection Reality

From QMS to QMSR: Navigating new enforcement, "Secure by Design" mandates, and the 2025 deficiency recap.

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