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Seven Ways Technology Reduces Maintenance Costs

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One large concern when maintaining a business’ facilities and assets is cost. Managing the costs of repairs, new parts, and personnel can present a challenge.

Traceability in Calibration

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Calibration is essential in almost every facet of industrial processes. The calibration process verifies test instrument accuracy by comparison with recognized standards, and measurement validity hinges on one crucial concept: traceability.

The Ugly Truth About Managing Design Controls on Spreadsheets

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At one point in my career, after managing design controls and risk management documentation, I decided to move on.

The Ultimate Guide to ISO 14155:2020 for Medical Devices

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Clinical investigations play an important role in your journey of bringing a medical device to market. While the relevant standards are often perceived as difficult and complex, having a good grasp of them makes the process less confusing.

How to Use Mistakes to Improve Quality

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We all make mistakes. Despite a vigorous editing process, there may even be one in this article!

My Research Can Help Protect You and Your Company From Hackers

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A scene from the movie Ocean’s 8 provides a surprisingly useful lesson on cybersecurity. The character played by Rihanna needs to hack into a security person’s computer. She looks up his social media to find he loves corgis.

The Return-to-Work Ultimatum Shaking Wall Street

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In an era when flexibility and autonomy are requirements, financial services leaders are ready to break the chains of traditional office norms.

Control Charts in Manufacturing: Are They Still Relevant?

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We are one year away from the 100th anniversary of the creation of the control chart: Walter Shewhart created the control chart in 1924 as an aid to Western Electric’s manufacturing operations.

How to Improve Biomed Technicians’ Quality of Life

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Growing medical equipment inventories and increasing technical complexity are demanding more than ever from the clinical engineering teams responsible for maintaining clinical assets.

Risk Management in ISO 13485

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In December 2023, the U.S. Food and Drug Administration (FDA) expects to issue its long-awaited overhaul of its Quality System Regulation (QSR).

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