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IAF CertSearch Team Identifies 20,000 Fake or Fraudulent ISO QMS Certs

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Credit: IAF CertSearch

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As of 2023, more than 27,000 medical device QMS certificates have been issued worldwide, providing confidence in medical devices.

Process Verification vs. Process Validation

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Photo by John Schnobrich on Unsplash.

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In a highly regulated industry like medical technology, manufacturing processes must undergo either process verification or process validation to ensure they’re consistently producing the correct result. The question is, which one should you use?

Top Five Challenges for Medical Device Integration

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Having appeared in the early 2000s, connected health technologies have gradually become a game changer in the healthcare industry.

Going Beyond Dust Hazard Analysis

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For owners and operators in the agricultural and food-processing industries, Jan.

How to Prioritize Cybersecurity Risks in Medical Devices

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Unpatched vulnerabilities

Protect Against Food Recalls With the Right Conveyor System

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With the threat of contamination from harmful pathogens such as salmonella, listeria, and e.

EU Regulation Is Driving Medical Device Manufacturers From EU Market

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In 2010 a medical device scandal in France set the stage for a new European Union medical device regulation that, according to most experts in the medical device community, may cause more damage than the problem it was intended to address.

Migrating Your QMS From Paper to AI

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Every company wants to succeed, but not all can say they meet the current requirements to do that. More than a focus on capital, business plans, or staff, a successful business in 2022 must operate digitally.

Food Expiration Dates Don’t Have Much Science Behind Them

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Florida’s outbreak of listeria has so far led to at least one death, 22 hospitalizations, and

How Pharma Quality Leaders Navigate Shifts and Instigate Change

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The pharmaceutical industry has seen significant upheaval and disruption during the past several years.

Pagination

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