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Explore Topics
- Valutek
- 7 October 2024
Risk Mitigation: Understanding PFAS in Cleanroom Garments
As discussed in Part 1: PFAS in Cleanroom Supply Chains, per- and polyfluoroalkyl substances (PFAS)...
- Valutek
- 6 September 2024
Are PFAS Chemicals Sneaking into Your Cleanroom Supply Chain?
If you’ve recently walked through the cookware section of your favorite store, you might have...
- Valutek
- 30 May 2024
Endotoxins: Strategies for Control in Life Science Environments
Medical device and parenteral pharmaceutical manufacturers are increasingly concerned with...
- Valutek
- 20 March 2024
Signs Your Cleanroom Design Needs a Refresh: A Guide to Re-evaluating Specifications
When any facility’s cleanroom is originally designed, experts evaluate many variables related to...
- Valutek
- 20 December 2023
Cleanroom Documentation Selection Fundamentals: Paper, Notebooks and Notepads
Paper is used daily in controlled environments to document work instructions, manuals, job orders,...
- Valutek
- 14 December 2023
Adhesive Mat Fundamentals: 3 Tips to Select & Install Cleanroom Mats
Adhesive mats remove contaminants from shoes, shoe covers, and cart wheels before entering...
- Valutek
- 12 October 2023
Best Practices: Designing a Gowning Room for Cleanroom Environments
For any cleanroom environment, the correct set-up of the gowning space is one of the most...
- Valutek
- 10 August 2023
Cleanroom Compliant Packaging: What You Need to Know
Before choosing the right supplier for your cleanroom products, consider the important role that...
- Valutek
- 30 May 2023
When Your Supplier Substitutes Cleanroom Products: Actions to Take
What if my cleanroom consumable supplier substitutes products?
Substitutions were commonplace...
- Valutek
- 25 May 2023
Exploring the Necessity of Requalifying Cleanroom Product Manufacturer
How often should you audit and requalify your current cleanroom consumable provider?
The frequency...
- Valutek
- 24 May 2023
How to Establish a Standardized Qualification Process for Cleanroom Consumable Manufacturers
Critical products need an objective and reproducible qualification process.
Cleanroom consumables...
- Valutek
- 15 May 2023
Unveiling Valutek's Industry Leadership: A Closer Look at 36-Month Rolling Lot Testing
Independent, repeatable testing is critical to qualifying cleanroom products and the first step to...
- Valutek
- 12 May 2023
The Significance of Qualifying Secondary Sources of Cleanroom Products
Global supply chain disruptions during the COVID-19 pandemic left controlled environment operations...
- Valutek
- 11 May 2023
Why Repeatable, Standardized Testing is Important for Cleanroom Products
Companies establish cleanroom operating procedures based on internationally accepted standards to...
- Valutek
- 10 April 2023
Why Qualifying a Backup Supply of Critical Products is Essential
A quality supplier should allocate inventory to current customers based on their historical usage...
- Valutek
- 6 April 2023
How Can Secondary Sources of Critical Products Safeguard Your Business Continuity?
Products that are critical to cleanroom operations merit a secondary source that serves as a backup...
- Valutek
- 29 March 2023
Ensure Your Controlled Environment Has a Reliable Supply of Critical Products
The COVID pandemic sent shockwaves through global supply chains, disrupting many markets,...
- Valutek
- 28 March 2023
3 Questions To Qualify Your Cleanroom Glove Supplier
Cleanroom gloves are supposed to be contaminant free. But not all gloves meet that requirement –...
- Valutek
- 28 March 2023
What Contaminants In Packaging Put Your Yields At Risk?
Packaging can contaminate cleanroom gloves and controlled environments, putting your production at...
- Valutek
- 27 March 2023
What Hidden Contaminants in Cleanroom Gloves Put Yields at Risk?
Your cleanroom gloves help to keep your controlled environment free of contaminants. Right?
How do...