Valutek Blog
Timely insights on productivity, best practices, and regulations—empowering you to boost yield and ensure compliance in your controlled environment.
Valutek
13
min read
Why Repeatable, Standardized Testing is Important for Cleanroom Products
Companies establish cleanroom operating procedures based on internationally accepted ...
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Valutek
8
min read
Why Qualifying a Backup Supply of Critical Products is Essential
A quality supplier should allocate inventory to current customers based on their ...
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Valutek
6
min read
Navigating Supply Chain Risks: How Secondary Suppliers Keep Your Business Running
Products that are critical to cleanroom operations merit a secondary source that serves ...
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Valutek
7
min read
Ensuring Business Continuity: Securing Your Critical Product Supply
The COVID pandemic sent shockwaves through global supply chains, disrupting many markets, ...
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Valutek
13
min read
3 Questions To Qualify Your Cleanroom Glove Supplier
Cleanroom gloves are supposed to be contaminant free. But not all gloves meet that ...
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Valutek
12
min read
Import Bans: How Unethical Labor Practices Impact Business Continuity
Global supply chain disruptions caused by the COVID pandemic led to bad actors in ...
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Greg Heiland
5
min read
U.S. Customs and Border Protection Seizing Cleanroom Glove Imports
Effective December 20, U.S. Customs and Border Protection (CBP) announced they will ban ...
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Valutek
11
min read
Standard Operating Procedure (SOP) Compliance Is At Risk!
Cleanroom Glove Covid-Impact White Paper And Survey Reveal Alarming Results, Offer ...
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Valutek
5
min read
How to Implement a Successful Cleanroom Glove Recycling Program
Recycling is consequential for the environment. Cleanroom gloves are the most commonly ...
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Valutek
1
min read
FDA Import Alert
The FDA issued the attached alert this past Friday, February 11th, 2022.
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About the Blog
Since 1988, Valutek has set the benchmark in innovative cleanroom solutions for life sciences, advanced materials, and academic research. Our blog offers timely insights on productivity, best practices, and regulatory trends.