Information provided by the manufacturer – Eisner Safety Consultants

IEC 60601, 4th Edition: What’s Changing and How to Prepare

leoeisner — Sat, 28 Feb 2026 21:33:00 +0000

IEC 60601-1, 4th Edition

Strategic Shifts and How to Prepare

Companion post to my Easy Medical Device podcast episode on IEC 60601-1, 4th Ed., focused on what is shifting across the Working Groups and what RA/QA, Design, Test, and Management teams should do now.

Most organizations will feel the impact long before any formal transition date. The practical shift is that evidence expectations are tightening, scope is becoming clearer, and the standard’s direction is being shaped now through Working Group outputs. Teams that treat this as a design input and planning topic today will avoid late-cycle surprises in test strategy, labeling, and documentation tomorrow.

Translate 4th Edition Direction into Organizational Action

Quick to read and easy to share across RA/QA, Design, Documentation, Supply Chain, Test, and Management. Use it to brief teams and kick off impact planning for IEC 60601-1, 4th Edition.

Your 4-Part Resource Kit

Listen to Podcast Episode Watch YouTube Interview EMD Magazine #2 Feature 4th ed. Survival Guide

Download One-Pager PDF

Use this one-page briefing handout to kick off internal alignment across RA/QA, Design, Test, Documentation, Supply Chain, and Management.

Read High-Level Overview

This newsletter provides a high-level overview of 4th Edition preparation themes, including transition timing, regulatory positioning, and early planning actions. For deeper technical shifts that drive design inputs and evidence expectations, use the podcast and the one-pager as the primary briefing baseline.

Why this matters for MedTech

The architecture is structured around 12 hazard-based Working Groups, with a much expanded and clearer scope. There are stronger expectations for intended use, user environments, software and PEMS, wireless coexistence, and emerging EMF exposure concepts. These changes will flow into design inputs, QMS documentation, labeling and IFUs, verification and validation evidence, and test strategy.

Across the Working Groups, changes are focused on

Scope and Essential Performance
User environments and intended use
Software and PEMS
International wireless coexistence expectations
EMF exposure concepts
Hazard-based structure

How to use this kit

Brief leadership using the podcast as the shared baseline.
Revisit your intended use, user environments, and understand the changing scope of the standard now.
Assign owners to track the Working Groups most relevant to your product and markets.
Track areas likely to affect:
- QMS documentation
- Labeling and IFUs
- Test strategy and test planning
- Design impacts
- Impact register – track what impact your company expects and what decisions you are making now

Related resources from my earlier Survival Guide

If you want the broader 4th Edition transition kit from my Survival Guide, it includes the MLVx one-pager, my MLVx webinar replay, a summary article, and the slide deck.

Want deeper analysis beyond LinkedIn?

My newsletter is where I publish longer-form breakdowns and structured updates that are not always fully posted on LinkedIn.

Subscribe to the ESC Newsletter Schedule a Call

If your team needs help mapping 4th Edition direction into design controls, QMS, labeling, or test strategy, my team at Eisner Safety Consultants can support you.

Medical Device Compliance & Certification Summit – Why It Matters?

leoeisner — Tue, 23 Dec 2025 23:30:37 +0000

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 – deeper design reviews, tougher pre-submission questions, 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 regulator expectations intersect in real programs.

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.

In-Person Training & Live Workshops

February 2–4, 2026
Carlsbad Inn Beach Resort, 3075 Carlsbad Blvd, Carlsbad, CA 92008

Designed for teams preparing new medical devices or diagnostics for market, working through recurring EMC or RF failures, or tightening FDA or EU MDR technical documentation ahead of submission or surveillance review.

Registration Summit Details

Who this summit is designed for

Electrical, EMC, RF, and systems engineers
Regulatory affairs and quality professionals
Product and compliance managers
Medical device and diagnostic startups preparing first submissions
Teams facing test failures, redesigns, or certification delays

What attendees will learn

How regulators evaluate standards application, not just test outcomes
Future impacts of IEC 60601-1, 4th edition concepts on design controls
Essential Performance and its role in risk management and review discussions
How EMC and RF strategies influence certification timelines
When IEC 61010 applies to diagnostic and laboratory equipment
Cybersecurity expectations under FDA and EU MDR
How guidance documents shape FDA and EU technical file expectations

How Eisner Safety Consultants Can Help

As regulatory expectations increase, delays are often caused by unclear standards interpretation, weak traceability between design decisions and requirements, and technical documentation that does not explain why choices were made.

Eisner Safety Consultants works with medical device, diagnostics, and combination device manufacturers every day to translate IEC 60601, IEC 61010, and related standards into practical design inputs, defensible test strategies, and documentation that aligns with FDA, EU, and other regulator guidance documents.

Registration Summit Details

From Engineer To “The IEC 60601 Guy” – Project MedTech Podcast

leoeisner — Sun, 19 Oct 2025 00:04:30 +0000

Podcast Feature

From engineer to “The IEC 60601 Guy” — my story and practical tips

I joined Duane Mancini on the Project Medtech Podcast to share how I became known for IEC 60601, why the series is a roadmap you can follow, and what 4th Edition changes mean for design, QMS, and documentation.

Episode 235

Listen on Web Open Spotify

A quick personal note

Nobody starts at the top as “The IEC 60601 Guy.” My path ran through early days at NASA, many years in test labs, and deep work in standards committees. What stuck with me is simple — stay curious, do the work, and show the work. That’s how we turn a dense standard into a practical plan.

Key takeaways from the episode

On the Project Medtech Podcast with Duane Mancini, M. Sc., I shared my genesis story of how I became known as The “IEC 60601 Guy”. Duane asked me to give listeners a 101 course on the IEC 60601 series, and I explained how I strive to “de-Greek” or demystify the standard series, and gave a preview of the big shifts coming in 4th Edition.

The “big picture” structure of the general standard, collateral standards, and particular standards

How lifecycle standards (risk management, usability, software) compare to type test standards in the 60601 family

Tangible changes to watch in the upcoming 4th Edition: clearer alarm requirements and impacts on design, QMS, & documentation

Why leaning on experts (internal or external) is key to getting this right for the impacts of 4th Edition

My goal is to “de-Greek” the process and show that IEC 60601 can be a roadmap , not a riddle

Whether you’re new to standards or a seasoned MedTech veteran, this episode shows how to approach IEC 60601 as a roadmap you can follow, instead of a riddle you can never quite solve.

What peers said

“If you want to know more about IEC 60601, Leo is the resource to go to … I recommend this episode to everybody working with medical electrical equipment.”

— Beat Keller

“Great to see how you became such an expert … I hope your story inspires young professionals to invest in becoming experts themselves.”

— Ronald Boumans

“It’s amazing that you covered the difference between process and test standards — there’s still a lot of confusion out there.”

— Tibor Zechmeister

Continue the discussion on this topic on LinkedIn

How We Can Help

If your team needs help with the IEC 60601 Series, or mapping the 4th Edition into your design controls, QMS, labeling, or testing strategy, my team at Eisner Safety Consultants and I are ready to support you.

Schedule a call with me, Leo, the IEC 601 Guy

IEC 60601-1, 4th Edition Survival Guide – Why It Matters For MedTech

leoeisner — Tue, 30 Sep 2025 09:23:00 +0000

IEC 60601-1, 4th Edition Survival Guide – Why It Matters For MedTech

The 4th Edition of IEC 60601-1 is no longer a future concern. Eleven of the twelve hazard fragments (WGs 37–48) have circulated Committee Drafts (CDs). All fragments have issued first CDs (WG 47 is at CD2), except WG 45 (Optical Radiation Hazards).

That means manufacturers, design houses, trade associations, test houses, and regulators must follow the working group outputs closely. If you cannot stay directly engaged in National or International (IEC) committees, you will need trusted expert guidance. These changes will impact design, QMS, labeling and IFUs, documentation, and test strategies.

Download the One-Pager: 9 Things RA/QA Leaders Must Know

Quick to read and easy to share with RA/QA, Design, Documentation, Supply Chain, Test, and Management. Use it to brief teams and kick off transition planning for IEC 60601-1, 4th Edition.

Your 4-Part Survival Kit

Download One-Pager PDF Watch Webinar Replay Summary Article Download Slide Deck

WG Status at a Glance

First-round CD comment periods are closed; the Compilation of Comments (CC) now drives edits in each WG. Expect a first wave of CD2s planned for early Dec 2025 after the Nov 2025 Milan work week, and a second wave following the Apr 2026 Shanghai meetings around Jun 2026. Stay current with CDs and CCs — or engage experts — because changes here will flow into design inputs, QMS, labeling/IFUs, V&V, and documentation.

Working Group	Key Document	CD Status	CD Comment Period	Compilation of Comments / Next Milestone
WG 37 – General requirements	62A/1628/CD	1st CD circulated Dec 2024	closed Feb 28, 2025	62A/1656/CC resolve by Dec ’25; iss CD2
WG 38 – Environmental & electromagnetic environments	62A/1630/CD	1st CD circulated Dec 2024	closed Feb 28, 2025	62A/1658/CC resolve by Dec ’25; iss CD2
WG 39 – User interface & alarm hazards	62A/1631/CD	1st CD circulated Dec 2024	closed Feb 28, 2025	62A/1659/CC resolve by Dec ’25; iss CD2
WG 40 – Materials hazards	62A/1632/CD	1st CD circulated Dec 2024	closed Feb 28, 2025	62A/1660/CC resolve by Dec ’25; iss CD2
WG 41 – Programmable electrical medical systems	62A/1675/CD	1st CD circulated Jun 2025	closed Sep 12, 2025	62A/1695/CC resolve by Jun ’26; iss CD2
WG 42 – Electrical hazards	62A/1676/CD	1st CD circulated Jun 2025	closed Sep 12, 2025	62A/1696/CC resolve by Jun ’26; iss CD2
WG 43 – Mechanical hazards	62A/1677/CD	1st CD circulated Jun 2025	closed Sep 12, 2025	62A/1697/CC resolve by Jun ’26; iss CD2
WG 44 – Thermal & mechanical energy hazards	62A/1673/CD	1st CD circulated Jun 2025	closed Sep 12, 2025	62A/1698/CC resolve by Jun ’26; iss CD2
WG 45 – Optical radiation hazards	—	No CD circulated yet	Next: issue CD1: TBD	Resolve by: TBD; Next milestone: compile CC after CD1
WG 46 – Ionizing radiation hazards	62A/1671/CD	1st CD circulated Jun 2025	closed Sep 5, 2025	62A/1693/CC resolve by Jun ’26; iss CD2
WG 47 – Electromagnetic exposure hazards	62A/1666/CD (CD2)	2nd CD circulated Jun 2025	closed Aug 29, 2025	62A/1689/CC discuss @ next mtg 2025-11-03
WG 48 – Electromagnetic disturbances hazards	62A/1672/CD	1st CD circulated Jun 2025	closed Sep 5, 2025	62A/1694/CC resolve by Jun ’26; iss CD2

9 things RA/QA leaders must know

One-Pager

Sean Smith captured nine essentials from the webinar (timestamps included):

Scope & Essential Performance; the boundaries for design, testing and compliance
Use Environments & Users; usability files and IFUs must match
Software Requirements Expanded; PEMS, SaMD, SIMD now covered
Collaterals Integrated; 1,000+ pages, one-stop standard
QMS Impact Areas; labeling, ISO 20417 reliance
EMC & Wireless Coexistence; higher RF fields, coexistence testing
Regulator Participation & Timeline; April 2030 + transition window
Hardware & Documentation Updates; alarms, usability, labeling, V&V
Immediate Actions; build an impact register, update labeling, begin EMC testing

The webinar replay

Watch Webinar

The replay provides the why — why regulators are focusing on scope and user environments, how expanded software/PEMS requirements shift the burden of evidence, and why wireless coexistence is no longer optional outside the US.

The summary article

Summary Article

This article organizes the hour-long webinar into a reference that RA/QA leaders and design managers can use to pinpoint pain points to focus on to avoid the fire drills of last-minute planning.

How to use this survival kit

Kick off a cross-functional session using the one-pager as the agenda
Watch replay segments together (software, EMC, labeling, etc.)
Assign owners for each of the 12 hazard Working Groups across RA/QA, Design, Test
Use the article as a quick reference to keep momentum
Track WG outputs and rely on your internal or external experts

one-pager for overview, the replay for context, the article for detail, and the slide deck for depth give your team a GPS starting point for 4th Edition readiness.

How We Can Help

If your team needs help mapping the 4th Edition into your design controls, QMS, labeling, or testing strategy, my team at Eisner Safety Consultants and I are ready to support you.

Schedule a call with me, Leo, the IEC 601 Guy

Keep the Conversation Going

Join the LinkedIn conversation around the replay post and comments — replay post and comments
See the earlier discussion thread and join the discussion: Major changes to IEC 60601-1, 4th Ed. are closer than you think
Explore more insights on my blog or listen to past podcasts

🎥 IEC 60601-1 4th Edition: Design Controls And QMS Impacts You Need To Know 📣📣

leoeisner — Mon, 25 Aug 2025 09:31:00 +0000

On August 15, 2025, I had the privilege of presenting the Impacts on IEC 60601-1, 4th Edition webinar as part of MLVx Friday In-Focus. The turnout was incredible, with more than 110 MedTech professionals from around the world joining. Startups, SMEs, large manufacturers, test labs, and regulators were all represented.

We unpacked the drivers and major changes in the upcoming 4th Edition, and the discussion didn’t stop when the webinar ended. Some of the most valuable insights came afterward in the LinkedIn conversations that followed.

See the replay post and comments here on LinkedIn
And the prior post: Major changes to IEC 60601-1, 4th Ed. are closer than you think

What the Industry Is Talking About

From the comments and follow-up conversations, four major themes stood out:

SME vs Large Corp Burden – Smaller companies worry the 4th Edition requirements could hit them harder than large corporations with more resources.
National & International Committee Involvement – Many are realizing that participating in standards development, even at the national level, gives manufacturers a seat at the table. Being involved internationally is even more powerful if you can swing it.
Rationale Behind Requirements – The Design Specification requires a rationale for each requirement of the standard. This is not fully addressed in Ed. 3.2, so the change should help improve industry understanding of the standard going forward.
Impacts on Design Controls, QMS, and Labeling – These changes are not just “paper exercises.” They will reshape how manufacturers approach design controls, QMS integration, and labeling processes across the entire product lifecycle.

Replay Video

If you missed the live session or want to revisit the details, here’s the full webinar replay:

Download the slides here

Why This Matters

As the IEC 601 Guy, I’ve been deeply involved in the development of IEC 60601-1, not just for this edition but also for the previous edition. The 4th Edition is shaping up to be one of the most impactful yet, especially in how it connects to design controls, supplier oversight, and QMS processes.

Conversations like these are important because they highlight the real-world concerns of manufacturers, regulators, and test labs. They help ensure implementation of the standard is proactive, not reactive.

How We Can Help

If your team needs help mapping these 4th Edition changes into your design controls, QMS, or testing strategy, my team at Eisner Safety Consultants and I are here to support you.

Schedule a call with me, Leo, the IEC 601 Guy. My team & I are here to support your needs.

Keep the Conversation Going

Standards only evolve when industry voices are active. I encourage you to:

Join the LinkedIn conversation: Replay post + comments
See the earlier discussion thread: Major changes to IEC 60601-1, 4th Ed. are closer than you think
Explore more insights on my blog: Standards Updates or see my previous Podcasts

Together, we can make sure these changes lead to safer devices, smoother regulatory pathways, and stronger compliance strategies.

Major changes to IEC 60601-1 are closer than you think

leoeisner — Fri, 15 Aug 2025 18:53:33 +0000

Once the 4th Edition is published, redesigns and QMS updates will be far more costly.

Direct insights from someone in the development of IEC 60601-1, 4th Edition

Get an insider’s view of the upcoming changes, their real-world impact, and how to prepare, from someone directly involved in developing the standard.

Event Recap – MLVx Friday In-Focus

On Friday, August 15, the MLVx Friday In-Focus with Sean Smith brought together Leonard (Leo) Eisner, The IEC 60601 Guy, and 110+ professionals from around the globe, including the UK, Romania, US, France, Switzerland, Germany, Finland, and Pakistan, representing medtech manufacturers, regulators, test houses, and standards developers.

We focused on the impact of IEC 60601-1, 4th Edition, the global standard that defines safety and essential performance for medical electrical equipment, and what’s coming that many companies are still not prepared for.

The highlight was an impromptu expert panel with leaders in risk management, software, cybersecurity, regulatory submissions, and combination devices. Together, we tackled questions from every angle, sharing real-world insights on design, testing, and compliance challenges. The discussion showed exactly what’s possible when top experts collaborate to help the industry prepare for disruptive change.

(Full presentation available for download at the bottom of this post.)

Unlock Your IEC 60601-1 Insider Advantage

Mitigate Risks: Spot disruptive changes early, prevent costly redesigns, and align documentation ahead of competitors
Accelerated Compliance: Seamlessly integrate evolving requirements into your development pipeline
Leadership Insight: The IEC 60601 Guy and our expert team track areas of interest for your organization based on draft documents
Behind Closed Doors: Access knowledge while it’s still being developed
Ready to Leap Ahead? Let’s turn this insider pipeline into your 4th Edition fast-track

+1-503-709-8328
EisnerSafety.com
Schedule a Free 30-Minute Web Meeting

If you missed the live session, this recap and presentation will help you understand what’s coming — and more importantly, how to prepare.

MLVx Impact of IEC 60601-1 4th Ed FINAL Vers 2025-08-15 compressed for website Download

🎩 Get your reviewer’s hat on – IEC 60601-1, 4th Edition Draft Fragments Have Dropped‼️ 🚀

leoeisner — Sat, 28 Jun 2025 01:09:39 +0000

Posted on LinkedIn June 19, 2025. Updated with extra blog content June 25, 2025.

Over the last two weeks – and with a Friday night (6/20/25 Geneva time – late) finale still to come – we’ve seen CD1s and CD2 (WG 47 ONLY) fly out for Fragments 5, 6, 7, 8, 10, 11, and 12 from WG 41 through WG 48, but for WG 45.

This is not just standards spring cleaning – these are foundational changes to the IEC 60601-1 General Standard, folding the Collateral standards into the core. If you have medical electrical equipment, medical electrical systems or software SaMD or SiMD you need to be aware of these changes. If you’re a manufacturer, test lab, trade association, Notified Body, Regulator or other interested party who owns a risk file… you need to review this.

These fragments cover hazards related to: • Electrical, mechanical, thermal, and fire • Software & PEMS (SaMD, SiMD, firmware, OS…) • EM Disturbance, wireless coexistence, ionizing radiation, and electromagnetic exposure (EMF)

The International comment deadlines start closing August 29th, with more due by September 12th. National deadlines close much sooner (does your summer holiday schedule conflict?)

Don’t wait for the FDIS – get involved now or get caught off guard later.

Read the full breakdown of all Working Groups, due dates, and what you should do now:

Here’s the who’s who of the Working Groups behind the fragments with CD1 to issue 20 July:

• WG 41 – PEMS (e.g., SaMD (Software as a medical device), SiMD (Software in a medical device), firmware, software, apps, OS, drivers) related hazards WG 41 link

• WG 42 – Electrical hazards WG 42 link

• WG 43 – Mechanical hazards WG 43 link

• WG 44 – Thermal and fire hazards WG 44 link

Other Fragments CD1s & CD2 have recently published – clock ticking to get your comments in:

• Fragment 11 – WG 47: Electromagnetic exposure hazards (not optical or ionizing but including SAR) WG 47 link CD2, closes 29 August

• Fragment 10 – WG 46: Ionizing radiation hazards WG 46 link CD1, closes 5 September

• Fragment 12 – WG 48: Electromagnetic disturbances (including wireless coexistence) WG 48 link CD1, closes 5 September

The early pack of CD1 Fragments released late last year

Fragments 1–4 and 11 from WG 37–40 & WG 47 were released as CD1 back on December 6, 2024, with comments closing February 28, 2025. You can still access them if you’re a National Committee member for SC62A or a WG participant. If not, consider joining — this is a major transformation, and early awareness = better preparation. Access link

Here’s a handy summary table of the IEC 60601 Fragments, their WG #s, their titles, the issue & close dates & more.

Who Should Be Reviewing

Design and Systems engineers
Risk management experts/leaders
Electrical & mechanical designers
Software designers (SaMD/SiMD, firmware, OS)
EMC/EMF compliance leads
Compliance engineers
Regulatory and quality teams
Usability & human factors engineers
Test labs
Trade Associations
Regulators
Notified Bodies
Other Interested Parties

What You Need to Do

Review the Drafts & the 4th ed. Design & Architecture Specs Now • Assign key experts by hazard/WG • Map against your design controls: Design Spec • Understand the architecture spec: Architecture Spec
Track IEV Part 880 Terms • Stay aligned with the evolving definitions: Terms & Definitions
Analyze Impact to Products • Run gap assessments • Identify implications for design, testing, and documentation
Submit Comments • Through your National Committees (ANSI, BSI, DIN, etc.) • Clear, technically sound feedback = meaningful influence
Update Design & Risk Inputs • Don’t wait for the final version to start aligning
Integrate Into Product Roadmaps • Work with R&D, QA/RA, and exec sponsors • Flag projects needing early adaptation
Engage the Right Experts • Join WGs or partner with someone who’s inside () • Stay active – your input now shapes what becomes final
Invest in Training • Get smart now to avoid surprises later

Don’t wait for the FDIS – get involved now or get caught off guard later.

Need help with standards?

We provide support for your design and development process for regulatory submissions.? Eisner Safety Consultants can help by

Assisting with strategic compliance planning for your medical electrical product lines,
Providing regulatory support when FDA or a regulator asks technical questions on your submission.
Identification of applicable standards, laws, regulations, guidances, and directives up front to support your design process effectively.
Design Documentation Reviews providing expert analysis supporting the design development process to avoid unnecessary design and development delays.
We provide EU, US, and other countries regulatory requirement reviews of standards, laws, directives, and guidance.
Providing support with Swiss MedDO, EU MDR, clinical evaluation assessment, NB remediation, STEDs, and more.
Interfacing with test houses for medical safety, EMC and arrange other testing.

Feel free to schedule a web meeting with Leo or contact us.

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

leoeisner — Mon, 31 Mar 2025 22:50:00 +0000

Join me, Leo Eisner, The IEC 60601 Guy, as I lead an interactive and fun workshop at the 10X Medical Device Conference in Newport Beach, Ca on May 7 – 8, 2025. Turn Medical Device Standards into Your Competitive Advantage, and discover practical strategies to leverage standards, avoid costly errors, and accelerate your product development cycle.

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.

I want to thank Sean Smith and his team from 10X for all his help and dedication for putting on this event. He is doing an amazing job and please contact him if you are interested.

Need help with standards?

We provide support for your design and development process for regulatory submissions.? Eisner Safety Consultants can help by

Assisting with strategic compliance planning for your medical electrical product lines,
Providing regulatory support when FDA or a regulator asks technical questions on your submission.
Identification of applicable standards, laws, regulations, guidances, and directives up front to support your design process effectively.
Design Documentation Reviews providing expert analysis supporting the design development process to avoid unnecessary design and development delays.
We provide EU, US, and other countries regulatory requirement reviews of standards, laws, directives, and guidance.
Providing support with Swiss MedDO, EU MDR, clinical evaluation assessment, NB remediation, STEDs, and more.
Interfacing with test houses for medical safety, EMC and arrange other testing.

Feel free to schedule a web meeting with Leo or contact us.

10x Humanizing MedTech: Breaking The Mould For Conferences

leoeisner — Tue, 11 Feb 2025 06:39:03 +0000

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?

The focus is on building meaningful relationships and tackling real challenges
Move through key stages of the MedTech lifecycle. Each workshop station focuses on critical topics such as:
- Regulatory Pathways
- Cybersecurity
- Engineering
- Product Development
- Market Access
- Reimbursement
- Commercialization

Join experts Carrie Britton, Matthias Fink, Sean Smith, Jan Gates, Angelina Lisandrelli, Jose Bohorquez, and others experts for a journey through the MedTech lifecycle – from ideation to marketed product. Each workshop represents a stage of this journey, offering opportunities to collaborate, ask questions, and exchange expertise.

Thank you, Sean for including me on this impressive list of experts for 10x this year!

Looking forward to seeing you in Newport Beach, CA. – Seats are limited

Join us for this very personalized experience and Joe Hage‘s Ice Cream Social

IEC 60601 Updates: What MedTech Need to Know for 2025 and Beyond Podcast

leoeisner — Thu, 12 Dec 2024 21:46:24 +0000

In this episode of the Global Medical Device Podcast, Etienne Nichols sits down with Leo Eisner, founder of Eisner Safety Consultants and a leading voice in IEC 60601 standards development.

We unpack the upcoming revisions to IEC 60601, 4th ed., focusing on the rationale behind these changes, their impact on medical device design, and how MedTech professionals can prepare for the future.

Leo provides insights into the intricate process of updating global standards, shares practical advice for compliance, and discusses the role of risk management in ensuring safer, more effective medical devices.

Key Points:

New Modular Approach:
- The updated standard adopts a modular approach (12 working groups focused on specific hazard areas).
- Simplifies updates by consolidating Collateral Standards into the General Standard.
- Aligns better with global regulations.
IEC 60601-1 4th Edition:
- Focuses on addressing various hazards including:
  - physical environment,
  - electrical,
  - thermal and fire,
  - mechanical,
  - user interface (usability, alarms, information supplied by the manufacturer & user interface aspects),
  - materials,
  - optical radiation, and
  - electromagnetic exposure hazards.
New Requirements:
- Introduces new international requirements for wireless coexistence and other cutting-edge technologies (e.g., gas pathways, user interface aspects).
Consolidation of Standards:
- Collateral standards are being consolidated to improve consistency and reduce the update cycle time for the 60601 series.
Timeline and Publication Dates:
- Expected timeline for the fourth edition is 2029-2030.
- Companies need to plan now, though the actual timeline may slip depending on various factors.
Benefits of Proactive Planning:
- Proactive planning and test preparation are essential for regulatory success.
- Staying informed and embracing continuous learning in MedTech are key factors for success.
Practical Advice for Compliance:
- Begin designing for new standards early, even before they are finalized. MedTech design cycles are long.
- Engage with industry groups and standards organizations.
- Use test planning to streamline development and meet regulatory expectations efficiently.
Engaging in the Standards Development Process:
- Manufacturers are encouraged to engage in the standards development process and submit comments.
- This proactive approach can help shape the standards and ensure they are practical and achievable.

These updates aim to enhance safety and performance while keeping pace with technological advancements. Manufacturers need to stay informed and prepare for the impact these changes will have on their product lines and quality systems.

Resources:

Design specification Outline for the fourth edition of IEC 60601-1

Architectural Specification For Safety Standards of Medical Electrical Equipment, Medical Electrical Systems, and Software Used in Healthcare

Only 5 of the 12 Fragments went out for CD on 6 Dec 2024, which were Working Groups (WGs) WG37, 38, 39, 40 & 47 (Fragments 1, 2, 3, 4, & 11 respectively). The status of each of these Fragments is noted below:

Fragment 1 (WG37) Status
Fragment 2 (WG38) Status
Fragment 3 (WG39) Status
Fragment 4 (WG40) Status
Fragment 11 (WG47) Status

The other 7 fragments will go out for CD approximately May ’25 (estimated schedule is my best intelligence). Fragments 5 – 10 & 12. You can look at the SC 62A Work Programme and find the Fragment number in the descriptions for each project on the first 12 projects of the Work Programme to find the status of each Fragment.

If you are a National Committee (NC) member and want to comment on the Fragment depending on your NC rules you may be placing your comments directly into the Online Standards Development (OSD) Platform for the Fragment. Other NCs are collecting the comments and then the NC Secretariat (or similar role) will be responsible for placing all the comments into OSD. Please check with your NC for your specific rules. Details about the OSD platform, How to use OSD, OSD resources (various training and other resources)

New terms and definitions which IEC 60601-1, 4th Ed. will be based on but other Technical Committees will adopt across the Healthcare sector to increase consistency – “International Electrotechnical Vocabulary (IEV) – Part 880: Electrical equipment, electrical systems and software used in healthcare” – IEC Website that has the schedule, list of draft documents. The CDV was released on 13 Dec 2024. If you are a National Committee Member of TC 1, TC 62, SC 62A, SC 62B, SC 62C, SC 62D, TC 65, TC 66, TC 76, TC 87, or SyC AAL you should be able to get access to this document and be able to comment on this document. This document is also being distributed for comment to ISO TC 210 and some additional ISO TCs .

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