Guidance on PDA 468 Validation Processes: Moist-heat sterilization is a widely used method for ensuring the safety and sterility of medical devices and pharmaceutical products. To ensure that these processes are effective, it is essential to validate them through a rigorous testing program. One important standard for validating moist-heat sterilization processes is PDA Technical Report
Capable of maintaining precise temperature-uniformity, our cold storage chambers deliver exceptional performance for applications where humidity control is not needed. This series of upright chambers can achieve temperature set-points as low as 30°C and is available in an extensive variety of sizes. Our cold storage chambers deliver strong volumetric (horizontal + vertical) uniformity of temperature,
Environmental Specialties low temperature freezers are custom built to customers’ unique size, temperature, and electrical control specifications. Their design helps conserve more energy and space than traditional storage methods. We custom design our Low Temp Walk-In (LTW) freezers according to your unique size, temperature, and electrical-controls specifications, as well as container type– from vials to
The Dry Heat Sterilization by Fedegari is the perfect solution for Bio-pharmaceutical Depyrogenation and Sterilization needs for Tools and glassware. FOD ovens, such as autoclaves, run batch processes and are the ideal solution for the sterilization of all those production lines in which the variability of products, batches and formats do not allow the use
Our Cleanroom manufacturers are starting 2021 with a great FREE Webinar. The presentation will take place on Thursday, January 7th, 2021 at 10 am CST. The goal of this webinar is to show you how you can get a mobile “Plug and Play” cleanroom as a permanent or temporary solution from design to build and
Innovation in a commodity market? When creativity is in your blood you cannot settle for basic innovation but you will explore new paths for revolutionary solutions. This was our goal when we started designing our first isolator. Process control Given Fedegari’s experience in different contamination control processes, our first priority was to assure the highest
Environmental Specialties is pleased to announce two innovations to our ES2000 Reach-In product line, which will be introduced as Environmental Specialties’ standard configuration on October 1, 2020. Both of these changes are in response to regulatory subjects that impact the core storage markets. First, the refrigerant used in our chambers will change from R404A to
Designed to maintain extremely low levels of particulates, such as dust, airborne organisms, or vaporized particles, our clean rooms are the ideal solution for specialized industrial production or scientific research—including pharmaceutical items, integrated circuits, and various specialized electrical components. Environmental Specialties (ES) engineers dry rooms with an obsessive level of chamber design, construction, performance, and
Fixing Print Registration, Upcoming "Tech-Tips Webinar" with Newman Labelling
Presented by Newman Labeling Systems
Is misaligned printing slowing your production or causing compliance headaches? Join our upcoming Tech-Tips webinar, where our labeling experts will walk you through common causes, quick fixes, and proven ways to keep your labels perfectly aligned — without costly downtime or equipment overhauls.
✅ Learn how to: Identify and fix print registration issues fast Optimize web tension and sensor placement Keep consistent results across label types and materials Reduce waste and downtime on your labeling line
Date & time: To be announced (you’ll receive full details by email after registration) Format: Live webinar + Q&A session
Our manufactures represented are major players, most offering you generations of consistent operation and production know-how!
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BFS Primary Advantages
Easier to maintain and monitor Aseptic conditions.
Inventory management is streamlined.
Storage of empty containers is eliminated.
More automated.
Parts washing and sterilizing is eliminated.
Less handling, Less Labor, Less Human intervention.
Filling and sealing all in one machine.
Greatly reduced facility size and utility requirements.
Customize your containers.
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We are pleased to announce that our company has recently been appointed as your Vibrac representatives throughout the Mid West.
Please do not hesitate to contact us for your new or existing cap torque testing requirements. We can help with new equipment selections, tooling, calibrations and service.