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  • Cleanroom Wipers

  • Cleanroom Gloves

    Cleanroom Gloves
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    Cleanroom Adhesive Mats
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    Cleanroom Apparel
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What you don’t know about flammable liquid use in your cleanroom…

  1. Procurement, storage and document control of flammable solvents is not a walk in the park. Chemical purchasing, storage, blending, dispensing, usage, and disposal require internal resources. Updated MSDS documentation must be keep on-site.


2. Bulk chemical blending and batch filling of squeeze bottles requires protective gear, a dedicated chemical handling fume hood, and a hazardous material plan. Liquid solvents represent a higher flammability risk “3”, versus a lower flammability risk “2” for the same solvent that is pre-saturated into a wiper substrate.


3. Operator exposure to an outgassing solvent in an air turbulent controlled environment is not an OSHA winning strategy. At normal room temperatures, liquid solvents give off enough vapors to form burnable mixtures with air, which represents an environmental safety risk. Outgassing volatile organic solvents represent an operator toxic inhalation risk.

Cleanroom-Cleaning copy

4. Disposal requirements of a flammable liquid. Good manufacturing practices recommends complete traceability of flammable solvents from cradle to grave.

insp with drums

Reduce your operator volatile organic liquid solvent exposure while improving your wiper efficacy with the Valutek Pre-Wetted Wipers solution.

How?  Valutek eliminates these non-value added activities that pose environmental liability and employee exposure risk to your organization.

  • Safety:  Eliminate the need for in-plant mixing, solvent handling & transport, and open solvent containers throughout your critical environment.
  • Environmental awareness: by eliminating solvent cans and excessive solvent use, Pre-Saturated wipes reduce needless evaporation, and overuse of volatile organic compounds
  • Efficacy: Wipers are wetted to exactly 38% of the total wiper sorbent capacity  to ensure ideal mix of dwell time, and cleaning capability. An “over-saturated” wiper cross-contaminates particles. Independent studies confirm that operators “over-saturate” their dry wiper.

  • Cost Reduction: Pre-Wetted wipers eliminate all the direct and indirect costs associated with solvent handling.
  • Vacuum sealed: All chemistry is driven into wiper substrate, ensuring uniform saturation from the wiper edge to center, and from the first to the last dispensed pre-wetted wiper.
  • Innovative 3 layer film:  Transparent packaging with a lower vapor barrier transmission rate versus traditional metallic film.
  • Custom cleaning Solution:  Choose the wiper substrate (non-woven & polyester), edge treatment (knife, laser, & ultrasonic), the chemistry and concentration you need.  Valutek will manufacturer to you specification with no minimum order, to ensure maximum shelf life.

Valutek Pre-Wetted Wipers Engineered Solution



Cleanroom Glove Packaging. Not all gloves are packed equal

Is your glove packaged in a dispenser box? Is it labeled ‘examination glove’ ?

If so, it is not suitable for a critical environment. Why? Boxed exam gloves are designed to protect the operator. Cleanroom Gloves are engineered to both protect the operator and your critical product.

cleanroom glove packaging


Controlled environment gloves are flat packaged in a critical environment with the cuffs all to one end in two stacks of 50 each, double poly-bagged 100 per pack, 10 packs per case in a carton liner to ensure product integrity. Boxed gloves are not.

Over 98% of thin-wall, powder-free gloves are used in medical / lab / industrial applications. Operators of controlled environments often unknowingly procure a glove not designed to their application. Powder-free lab / industrial / medical grade boxed gloves are not suitable for a controlled environment because:

  • Boxed gloves are powder-free, not particulate-free. Uncoated chipboard dispenser boxes shed particles, and contaminate the powder-free gloves.
  • Dispenser boxes force operators to contaminate glove when donning. Operators’ bare hand should only make cuff contact.
  • Additives and fillers are often used in boxed gloves which reduce ESD compatibility (surface resistivity), and negatively impact glove cleanliness.
  • No post-processing to reduce surface contamination left from the dipping process

Engineered to protect your Product, Process & Operator

Valutek’s gloves are packed in double poly bags, vacuum sealed, flat packed in carton boxes and with a carton liner. All gloves are critical environment compatible, lot traceable with retention samples held in quality control for 36 months from date of manufacturing.

Vacuum seal benefit: better storage, no particulate release, no ESD issue

cleanroom glove packaging


Robot Automated Transportation for Cleanrooms Revealed

Ortner, a factory automation specialist, and its partner MetraLabs Automation, a provider of freely navigating autonomous mobile robots, have introduced their jointly-developed mobile robot, SCOUT at SEMICON West.

SCOUT has been specially developed for the flexible and automated transportation of materials in semiconductor fabs and other clean production environments.

SCOUT navigates autonomously, without any kind of guidance system and communicates via WiFi and operator GUI to issue new transport jobs and show important status information like its current position. The robot is cleanroom suitable up to ISO class 3 / US FED class 1 and has more than 5,000 km of autonomous navigation in clean rooms, which proves its reliability.

Thanks to its compact size and reliable sensor technology, SCOUT can be used safely in areas where people and machines work closely together,” explains Matthias Merten, CEO of MetraLabs Automation, Inc. “This makes SCOUT an ideal alternative in cases where a permanently installed transport system such as a rail or a conveyor system cannot be implemented or would be too expensive…

Click Here to Read the Full Article.

Space For All: Small, Cheap Satellites May One Day Do Your Bidding

Someday, swarms of satellites the size of a tissue box will be snapping pictures, taking environmental readings and broadcasting messages from orbit — but the entities controlling those satellites won’t be governments. Instead, they’ll be hard-core hobbyists and elementary-school students, entrepreneurs and hacktivists. In short, anyone who can afford a few hundred dollars to send something to the final frontier. The technology for this outer-space revolution already exists: It’s a type of satellite known as a CubeSat, which measures just 4 inches (10 centimeters) on a side. The CubeSat phenomenon started out as an educational experiment, but now it’s turning into a crowdsourcing, crowdfunding movement of Kickstarter proportions. And not even the sky is the limit…

Click Here to Read the Full Article.

How an Outbreak Changed Compounding Pharmacies: The Ophthalmic Side Effects

Compounding pharmacies have been vital to retina since specialists began using bevacizumab (Avastin, Genentech, South San Francisco, CA) to treat AMD.

With last year’s fungal meningitis outbreak traced to a compounding pharmacy in Massachusetts, these facilities have come under increased scrutiny. Two major compounders in the ophthalmic drug space have reviewed their own processes and made changes to allay the concerns of physicians, while the accrediting organization for compounding pharmacies is handling increased requests for inspections.

Last October, compounding pharmacies came under increased scrutiny when problems with sterile conditions arose at the New England Compounding Center (NECC), leading to the outbreak that resulted in 696 cases of meningitis and 45 deaths in 20 states…

Click Here to Read the Full Article.

Better FDA Oversight is Needed for Prescription Safety

But one segment of the pharmaceutical industry has been carved out of the FDA inspection process. Compounding pharmacies, which create customized medications from scratch, are regulated by state boards, and sometimes not closely enough. Most are professionally run operations that serve an essential role in medicine. But as two recent incidents have proved, it is too easy for rogue drug manufacturers to exploit an oversight vacuum and jeopardize patients’ safety.

An outbreak of deadly fungal infections identified in September was traced to the New England Compounding Center in Massachusetts. Regulators said the place was operating more like a drug manufacturer than a traditional compound pharmacy, which works with physicians to produce small quantities of medications. The contaminated drugs that were mass produced by the Massachusetts firm sickened more than 700 persons and killed 58 others.

More recently, illnesses in four states have been linked to the Main Street Family Pharmacy in Tennessee. Regulators have cited the operators with multiple violations, including the discovery of spiders in the “clean room” where sterile drugs are compounded.

This risky behavior must end. Fortunately, a bipartisan group in…

Click Here to Read the Full Article.

A Cost-Effective Option for Pharmaceutical Compounding

Hospital pharmacies face a stiff challenge as the fallout over the recent meningitis outbreak caused by tainted compounding continues: As scores of other vendors shut their doors because they failed FDA inspections, how does a hospital ensure the adequate flow of crucial admixtures?

One solution is to bring more of the sterile compounding workload back into the hospital. But this strategy has its own risks and challenges, including ensuring United States Pharmacopeia (USP) <Chapter 797> compliance, adjusting staffing and workflow, and building expensive new clean rooms and buying other high-ticket equipment and technologies. Another roadblock: steering clear of the regulatory minefield surrounding beyond-use dating (BUD)…

Click Here to Read the Full Article.


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