For ISO 14644 compliance, all particle counting equipment requires a calibration certificate.
Are you in compliance? Do you qualify for an exemption? Generic signage no longer adheres to recent Proposition 65 updates. Custom order Accuform signage is now available from PAC. Our specialists tailor hazard signage for your storage, entrance, and production areas.
New reports indicate that alcohol hand washes and sanitizers may be losing the hygiene battle against super strains of Enterococcal bacterial. Educating practitioners and patients on the when, where, and why of hand sanitation in healthcare has led to a pronounced decline in MIRS and HCAIs for the greater part of the last 20 years. Meanwhile, “what” we wash our hands with has required little examination.
Genuine linoleum is a 100% biodegradable material composed of linseed oil, pine resin, cork, wood, pigment, and limestone. Depending on material construction, it is known to have antistatic properties which mitigate some triboelectric charges that cause zaps and static buildup.
Find hand dryers, laboratory receptacles and cleanroom mirrors. New from CleanPro with quick ship options.
ISO 13485 is designed for use throughout the life cycle of a medical device. It supports each stage of medical device development and operation from initial concept to production and disposal. The standard helps internal and external parties certify and validate processes which maintain the stability of quality management systems (QMS).
Modular cannabis grow room designs improve the longevity of grow room construction. Likewise, portable prefab grow rooms allow for more adaptable configurations when expanding, relocating, or re-purposing a grow room. There are also a number of tax and legal advantages when construction is non-permanent. Prefab modular grow rooms are cost-effective without the inconvenience of conventional “stick-built” construction.
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Are the terms sterile and aseptic used interchangeably? Is a cleanroom sterile? What is aseptic processing?
Cleanroom particle counters and anemometers offer portability, accuracy, and easy use. The self-contained devices allow local and off-site testing of air quality, air speed, HVAC efficacy.
Pre-engineered fabrication consolidates scheduling with minimal disruption and fewer variables. Difficult or expensive upgrades avoid overbearing noise, construction artifacts, and minimize if not eliminate the burden on facility staff for project management.
USP Chapter 797 cleanroom design requires that facilities pressurize non-hazardous compounding and storage areas. ISO 5, 7 and 8 environments support primary engineering controls, buffer rooms, and ante-rooms.
New USP guidelines may present challenges for compounding facilities. Some facilities need infrastructural and mechanical modifications for compliance. System evaluation includes duct systems, HEPA fan filters, differential pressure standards, air monitoring, and external air exhaust equipment.