Are Medical Device Companies Getting the Voice in the ISO Standards? | 2min snip from Global Medical Device Podcast powered by Greenlight Guru

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QMSR: The Future of FDA's Quality Management System Regulation for Medical Devices

Global Medical Device Podcast powered by Greenlight Guru

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Are Medical Device Companies Getting the Voice in the ISO Standards?

80 plus percent of medical device companies are 50 or a fewer employees. It is hard to be involved with standards committees iy, thect. Those who do that's oftentimes their full time job. smaller sized companies may not be afforded the luxury of being able to hire a person whose sole responsibility is to be involved in and guidances and regulations,. an standards creation.

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FDA has proposed a new rule to align its Quality System Regulation (QSR) with ISO 13485:2016, the international standard for medical device quality management systems. How will, what's being referred to as Quality Management System Regulation (QMSR), affect the medical device industry and regulatory bodies?

In this episode of the Global Medical Device Podcast Jon Speer and Etienne Nichols talk to Mike Drues of Vascular Sciences and George Zack of Two Harbors Consulting about the changes unfolding and the pros and cons of harmonization between QSR and ISO 13485:2016—a standard not governed by FDA.

Some of the highlights of this episode include:

The FDA is not expected to adopt ISO 13485 or any other standards across the board. Instead, it will take a piecemeal approach. Any future revisions to the 2016 version of the standard would need to be evaluated before becoming part of U.S. regulations.
How often are periodic changes and updates made to QSR, ISO standards, and FDA guidances? Do changes even need to be made or are they a waste of time and money? Good regulation is agnostic of time and technology.
Government bodies in different parts of the world want to protect their citizens. Will there ever be global harmonization for quality? Are the most important principles of quality a function of geography? No, quality is quality.
The timeline to transition is one year, but companies and inspectors may need or want more time due to a limited number of resources and notified bodies.
If a company does what it should do for the safety and efficacy of medical devices, it should really be a tiny or no leap at all to make changes. The only changes are in the paperwork and forms.
Medical device professionals should know about ISO 13485. If they do not know about this standard, whether it is required or not, that could be a problem.
For those adhering to ISO 13485, if there are new requirements that make sense from a biology and engineering perspective, that’s the way to do something.

Memorable quotes from this episode:

“They are not going to adopt ISO or any other standards across the board. They’ll take sort of a piecemeal approach, and I think that makes sense.” Mike Drues

“When was the last time that the design control guidance was updated since it was created in 1997? The answer is, never. That guidance has remained exactly the same.” Mike Drues

“Good regulation is timeless.” George Zack

“While it might not be a huge shift, I think it is a step in a direction of many steps toward some sort of global harmonization.” George Zack