• 
  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
• 22 May 2023

5 Reasons to Trust Valutek as Your Critical Environment Consumables Manufacturer

Your critical environment consumables are used in every step of your cleanroom operation, with your...

• 
  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...

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  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
• 21 February 2023

Cleanroom Glove Selection Fundamentals Part II : Cleanliness Requirements

Often customers ask us for a “Class 10 cleanroom glove.” The truth. It doesn’t exist. Class 10 is...

• 
  Valutek
• 21 February 2023

Cleanroom Glove Selection Fundamentals - Part I : What You Need to Know

Selecting the most appropriate cleanroom glove can seem complicated. If you are trying to match...

• 
  Valutek
• 2 November 2022

Standard Operating Procedure (SOP) Compliance Is At Risk!

Cleanroom Glove Covid-Impact White Paper And Survey Reveal Alarming Results, Offer Solutions.

There...

• 
  Valutek
• 13 January 2022

FDA Import Alert

The FDA issued the attached alert this past Friday, February 11^th, 2022.

• 
  Greg Heiland
• 13 January 2022

U.S. Customs and Border Protection Seizing Cleanroom Glove Imports

Effective December 20, U.S. Customs and Border Protection (CBP) announced they will ban imports of...