When searching for "True" HEPA filters, H13, or IEST rated HEPA filters, not all classifications of HEPA filters are created equal. There are numerous groups and classifications that further distill HEPA performance ratings into more specific performance categories.
Terra’s HEPA and ULPA filters are specially designed for use in cleanrooms, labs, and precision assembly areas. They come in a wide range of sizes for use in Terra work stations, cleanrooms, and many other applications. They can also be used as final filtration in standalone purification systems.
Check out our list of Dos and Don’ts in a cleanroom, a summary of cleanroom best practices for making the controlled environment function at peak performance. These are good resources for new cleanroom operators or those unsure about what steps to take in a cleanroom environment.
Cleaning a laminar flow hood sounds like a self-explanatory task, but there are plenty of factors to consider when the stakes of sterilization include the integrity of your products. Even more importantly, a clean laminar flow hood helps ensure the safety of patients and consumers on the receiving end of those products.
Most cleanroom professionals understand that Fan/Filter Units (FFUs) capture contaminants that degrade particle-sensitive samples. But they also remove bacteria, viruses and mold spores that contribute to a host of infections.
With the threat of superbugs on the rise in medical facilities, sterilization has never been more crucial. Superbugs, or drug-resistant bacteria that cannot be killed by standard antibiotics, have the potential to cause infections that are increasingly difficult to cure. The number of deaths related to these bacteria is decreasing. But the bugs, and the danger, remain present.
Until new cures are developed to battle bacteria, the solution to preventing the spread of germs is to update cleanliness procedures in hospitals, pharmaceutical manufacturing facilities and other places where drugs are regularly developed or used. Hand-washing can push back against the threat, but
Many manufacturers face the challenge of maintaining sterile products and processes. In most cases, there’s no one-size-fits-all solution. Highly effective sterilization technologies like ethylene oxide gas (EtO) or hydrogen peroxide vapor carry substantial risk and often come at a high cost. Frequent manual wipe-down with IPA or other cleaning agents is much less expensive but introduces difficulties related to operator training and process documentation and consistency. In many cases, the challenge amounts to managing multiple technologies that provide microbial control throughout widely differing processes—while minimizing costly disruptions for bioburden testing or decontamination routines.
Fortunately, ultraviolet sanitizing technology provides a range of safe, cost-effective disinfection measures that simplify this task, whether employed as a stand-alone measure or as part of a broader
Manufacturers invest hundreds—even thousands—of dollars per square foot of cleanroom space to meet ISO-proscribed particle counts. Shouldn't the same standards be required of the people who enter and potentially contaminate this ultra-clean environment?
Proper cleanroom garments, including hoods, face masks, booties and gloves, help to contain particles that people emit. Yet improper gowning procedures can negate your investment in cleanliness and threaten yields of sensitive semiconductor devices. Once a garment is contaminated—violated by contact with a dirty surface—it spreads particles everywhere it goes.
You can train personnel on proper garmenting procedures, but how do you guarantee compliance? A violated garment doesn't set off alarms, and few facilities can afford quality control monitors to supervise every person through every washing and dressing stage. Yet if strict controls are not obser
Controlling microbial contamination is one of the leading concerns in research, clinical, and medical facilities. Microorganisms (hazardous or not) can put personnel, patients and caregivers at risk. In hospital and medical facilities, patients are often immuno-compromised or have serious conditions that make them particularly susceptible to opportunistic microbes or secondary infections.
For these reasons, many products are available for decontamination of these critical spaces. There are differences in product effectiveness, cost, potential residual damage and operation
Whether lab technicians like it or not, cleanrooms are exposed to contaminants. Adulteration can occur from personnel, equipment, or even incorrect decontamination processes. Since many cleaning methods exist, it’s important to select one that’s best for your application; an careless technique may redeposit contaminants onto surfaces rather than take them away. Understanding particle-to-surface bonding (electrical, physical, or chemical) is one of the first steps to optimal cleaning efficiency. Keep reading for more tips that ensure your cleanroom remains clean.
“Wet cleaning” removes contamination with the use of a cleaning fluid. In some cases, wiping will move particles, but fail to remove them. Therefore, wet cleaning is typically implemented when wiping is not enough to overcome the particle adhesion. Cleaning solutions include a number of chemical choices; bas
Sterilization is a process designed to destroy and remove all forms of life present in a certain region. It’s accomplished by use of physical or chemical means. Autoclaves, for example, steam sterilize by high pressure and heat (250°F/121°C at the low end).
Another sterilization-by-heating technique uses infrared to kill microorganisms in a few seconds using temperatures up to 1500°F/815°C. On the chemical front, hydrogen peroxide can break down cellular tissue.
Sterilization can also be used to elimi
The cleaning and sterilization of laboratory, clinical, surgical and compounding equipment is necessary to ensure patient safety and accurate results. In research laboratories, improperly cleaned or sterilized glassware and instruments opens the door to unwanted contaminants. Contaminated objects can also endanger laboratory personnel through exposure to mutagenic or toxic substances.
In clinical labs, contamination can lead to erroneous test results, jeopardizing patient treatment regimens or diagnoses. In surgical and pharmaceutical facilities, improper sterilization of equipment or compounding preparations can expose patients to a wide range of microbes and endotoxins. Thus, labs must develop and document washing and sterilization protocols that produce reliable results and ensure safety.
According to a Frost and Sullivan survey published in Lab Manager Magazine, 60% of laboratory budgets are spent on consumable products. Another 30% of the total budget i