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Facility Inspection Articles & Analysis

5 articles found

Why Low-Cost Medical Drainage Bags Could Actually Cost You More

Why Low-Cost Medical Drainage Bags Could Actually Cost You More

At first glance, a cheaper drainage bag may seem like a smart move for a tight budget. But procurement teams know the real cost of a product goes far beyond the price on the invoice. When medical drainage bags fail to perform, the ripple effects show up in the form of surgical delays, patient dissatisfaction, and even infection risk. Discover the hidden costs of low-quality drainage ...

ByRemington Medical Inc.


How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

As spring arrives, so does a renewed focus on cleaning, quality, and process validation in pharmaceutical facilities. Whether it’s a routine seasonal turnover or preparation for ramped-up production cycles, spring is a critical time in the pharmaceutical industry for equipment maintenance, cleaning validation, and ensuring product purity. Behind every cleanroom, batch reactor, or ...

ByFluorostore


Spring Clean Starts in the Lab: How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

Spring Clean Starts in the Lab: How Fluoropolymer Tubing Supports High-Purity Pharmaceutical Production

As spring arrives, so does a renewed focus on cleaning, quality, and process validation in pharmaceutical facilities. Whether it’s a routine seasonal turnover or preparation for ramped-up production cycles, spring is a critical time in the pharmaceutical industry for equipment maintenance, cleaning validation, and ensuring product purity. Behind every cleanroom, batch reactor, or filtration ...

ByFluorostore


What is Pharmaceutical CGMP Manufacturing?   

What is Pharmaceutical CGMP Manufacturing?  

This article delves into the nuances of CGMP manufacturing, including pilot scale-up and commercial manufacturing aspects, along with the facilities and services that support these crucial processes. What is Pharmaceutical CGMP Manufacturing? ...

ByCD Formulation


Why FDA Compliance Needs A Defined CAPA Process.

Why FDA Compliance Needs A Defined CAPA Process.

Food and Drug Administration (FDA) Medical Device Enforcement and Quality Report, the agency has increased annual inspections at manufacturing facilities by 46 percent since 2007. In 2017 alone, the FDA conducted 2,592 inspections, the report said, with foreign facility inspections increasing by 243 percent in ...

ByEtQ, LLC

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