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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.

Food Processing: Automatic Scraper Strainers Protect Critical Membrane Systems

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The use of membrane technology as a processing and separation method in the food industry is gaining wide application for demineralization, desalination, stabilization, separation, deacidification, purification, and reducing microbial load.

Four Factors to Consider When Buying an Ultra-Low Temperature Freezer

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Ultra-low temperature freezers became popular due to the storage of Covid-19 vaccines, but they have been important components of laboratories for many years.

The Value of Risk-Based Supplier Inspections in Pharma Quality Management

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Quality management is essential to the growth and performance of any organization. It’s a valuable resource in the effort to ensure that products and services satisfy the highest quality requirements and deliver positive customer results.

Staying Ahead of ICH E6(R3) Good Clinical Practice Guidelines

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By now, it’s no secret that good clinical practice (GCP) guidelines used by FDA inspectors are expanding. These GCP guidelines are developed by the International Conference on Harmonization. The ICH last revised its GCP document, called ICH E6(R2), in 2016.

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