Keep the Patient at the Center: My Full Week at IMSC26 (and Why Getting Ahead of IEC 60601-1, 4th Edition Is Really About People)

Keep the Patient at the Center: My Full Week at IMSC26 (and Why Getting Ahead of IEC 60601-1, 4th Edition Is Really About People)

Two events across Greater Boston, and the most energizing week I have had in MedTech in a long time. It started in Boxborough with the TÜV Rheinland North America IEC 60601-1, 4th edition seminar, then rolled into four days at IMSC26 in Boston: a 4-hour CEF/CEP workshop, a 45-minute session to a packed room plus a virtual audience, and a stack of hallway conversations I am still thinking about.
What I did not expect was how often the human side moved to the front. A patient’s own account of life on the receiving end of a device. A regulator speaking candidly about where the FDA is headed. Combination products, risk management maturity, usability, and the quiet, unglamorous work of writing the standards themselves. Different rooms, different speakers, the same gravitational pull back to the patient.
So I wrote up the moments that earned a place in my electronic notebook, what they mean for teams designing and testing products right now, and where IEC 60601-1, 4th edition fits into the picture. Less a conference summary, more a field report from someone who has spent 30-plus years in this work and still came home with a full page of new ideas.

Medical Device Compliance & Certification Summit – Why It Matters?

Medical Device Compliance & Certification Summit – Why It Matters?

Medical device and diagnostic compliance expectations are shifting earlier in the product lifecycle. IEC 60601 and related standards are no longer something teams can “handle at test.” Regulators increasingly expect standards interpretation, risk decisions, and test strategy to be visible and justified during design reviews and technical documentation development.

This shift is showing up in real ways – through tougher design reviews, deeper questions during pre-submission interactions, and increased scrutiny of how standards were applied, not just whether a final test report exists.

To address this reality, Eisner Safety Consultants (ESC) is working with Nemko to deliver a three-day, in-person Medical Device Compliance & Certification Summit focused on how standards, testing, and regulatory expectations intersect in real programs.

This is a focused, three-day program for engineering, regulatory, and compliance teams navigating IEC 60601, IEC 61010, EMC and RF requirements, certification strategy, and regulator guidance documents across FDA, EU, and other markets.

Join me for an Interactive Workshop Identifying Standards, Guidances, & Turn Standards into Your Competitive Advantage @ 10X

Join me for an Interactive Workshop Identifying Standards, Guidances, & Turn Standards into Your Competitive Advantage @ 10X

Don’t make the 5 costly mistakes companies make with Medical Device Standards. Learn from the IEC 60601 Guy himself.:

Late Identification of Applicable Standards: Leads to expensive redesigns and delayed timelines

Ignoring Expert Standards Guidance: Results in regulatory rejections and costly resubmissions

Unprepared Risk Management File for Testing: Risks unnecessary costs due to lack of strategic planning for compliance.

Unprepared Regulatory Submissions: Leads to costly setbacks and market-entry delays

Underestimating Education and Training: Creates knowledge gaps, increasing errors and compliance risks.

ISO 20417, 2nd DIS Breaking News from Tokyo Meeting 📣📣

ISO 20417, 2nd DIS Breaking News from Tokyo Meeting 📣📣

👉 ISO TC 210 WG2 met in Tokyo, Japan 🇯🇵 on 4 – 5 March 2025. 👉 WG2 meeting focused primarily on resolving the National Committees (NCs) comments received on the ISO/DIS 20417, 2nd ed. Changes proposed: 👉 Add reference

10x Humanizing MedTech: Breaking The Mould For Conferences

10x Humanizing MedTech: Breaking The Mould For Conferences

Join us for the fifteenth 10x Medical Device Conference on May 7 to 8, 2025 – Hyatt Regency Newport Beach, CA What’s 10x 2025 about you ask? Join experts Carrie Britton, Matthias Fink, Sean Smith, Jan Gates, Angelina Lisandrelli, Jose