In this episode of the Global Medical Device Podcast, host Etienne Nichols continues his conversation with regulatory expert Mike Drues in part two of their series on home use medical devices.
The discussion centers on critical topics such as labeling, usability challenges, and the future of medical devices in home settings. They explore how these devices, increasingly used by non-healthcare professionals, face unique hurdles such as user training, environmental factors, and technological concerns like cybersecurity and data security.
Together, Etienne and Mike also delve into how regulatory frameworks need to adapt for home use, and they highlight potential future issues with devices as AI and robotic assistance grow in prominence.
Interested in sponsoring an episode? Click here to learn more!
Listen now:
Love this episode? Leave a review on iTunes!
Have suggestions or topics you’d like to hear about? Email us at podcast@greenlight.guru.
Key timestamps
- [02:20] - Recap of Part 1 & Introduction to Home Use Devices: Mike revisits key topics from part 1, focusing on why home use devices matter.
- [10:45] - Defining the Intended User and Environment: Discussion about how labeling must account for who will use the device and where.
- [15:30] - Technological and Environmental Challenges for Home Use Devices: Exploring temperature, humidity, and power inconsistencies affecting performance.
- [30:05] - Reprocessing and Cleaning Devices at Home: The challenges and risks associated with reusing and cleaning devices like CPAPs.
- [40:15] - Usability Testing & Human Factors: Importance of considering non-healthcare users when designing home devices.
- [55:12] - Cybersecurity Risks in Home Devices: The growing significance of data security and strategies for protecting devices in non-clinical settings.
- [1:05:30] - Post-Market Surveillance and Reporting for Home Devices: The complexities of tracking device performance and recalls when used in home environments.
Top takeaways from this episode
- Increasing Use of Home Medical Devices: Patients are increasingly managing their own health at home, necessitating devices that are user-friendly and adaptable to various home environments.
- AI & Robotics in Home Devices: With the rise of AI and robotic assistance, the definition of an "intended user" is evolving, requiring future-proof regulatory considerations.
- Data Security: As more devices become connected, cybersecurity is becoming a top priority, particularly for critical, life-sustaining technologies.
Practical tips for MedTech professionals
- Understand the End-User: When designing devices, consider that patients, not healthcare professionals, will be the primary users. Usability is key.
- Incorporate Environmental Testing: Take environmental factors like humidity, power outages, and storage conditions into account during the device development phase.
- Push Updates Automatically: For connected devices, push software updates automatically to mitigate cybersecurity risks, rather than relying on users to pull them.
MedTech 101
What are home use medical devices?
Home use medical devices are defined as devices intended for use in environments outside of traditional clinical settings, such as homes, schools, and offices. These devices must be designed to accommodate non-professional users, accounting for factors like usability, environmental conditions, and ease of maintenance. Understanding these nuances is essential for developing safe and effective devices for a growing market.
Related links
Memorable quotes from this episode
- "When we talk about intended users, we must shift our thinking from healthcare professionals to patients. Designing for non-clinicians is crucial because usability directly impacts safety." – Mike Drues
- "If your device has to be recalibrated, why not have a mechanism that disables it when calibration is overdue? That’s a much stronger safeguard than relying on users to remember." – Mike Drues
- "Cybersecurity is a growing challenge in home devices. It’s not just about protecting personal data—imagine if a critical medical device was hacked." – Etienne Nichols
Audience feedback
Love this episode? Leave a review on iTunes! Have suggestions or topics you’d like to hear about? Email us at podcast@greenlight.guru.
Sponsors
- Greenlight Guru: Is your QMS holding you back? Greenlight Guru is THE eQMS built for medical device companies to accelerate success and ensure compliance with FDA, ISO, and EU MDR requirements. Streamline your quality processes and focus on innovation. Visit www.greenlight.guru to learn more!
- Rook Quality Systems: Ready to ensure your QMS is audit-ready? Rook Quality Systems offers comprehensive QMS audits and training tailored to your organization’s needs. From gap analysis to corrective actions, Rook helps you maintain compliance and efficiency. Schedule your audit at www.rookqs.com.
About the Global Medical Device Podcast:
The Global Medical Device Podcast powered by Greenlight Guru is where today's brightest minds in the medical device industry go to get their most useful and actionable insider knowledge, direct from some of the world's leading medical device experts and companies.
Like this episode? Subscribe today on iTunes or Spotify.