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ANALYTICAL AND LABORATORY EQUIPMENT


BIO-DECONTAMINATION CYCLE TIME REDUCED BY 20% B


ioquell has created the capability to calibrate low-level hydrogen peroxide vapour instruments accurately at 1 part per million (1ppm), helping to reduce cycle times by approximately 20%. The company is now able to calibrate to a published Occupational Safety & Health Administration (OSHA) method at the critical concentration point, ensuring safety of employees while optimising the cycle. It is important that any low-level


hydrogen peroxide sensor, used to determine the end of a decontamination cycle, is accurate. This is to ensure the safety of the personnel entering the area as well as to optimise the cycle time. The present calibration methods used by sensor manufacturers are often not performed with hydrogen peroxide vapour, and are not conducted at a vapour concentration at the critical value of 1ppm. Testing and experience have shown that inaccuracies can unnecessarily prolong decontamination cycles by up to 20%. Bioquell now has a calibration capability able to expose


these sensors to a 1ppm hydrogen peroxide vapour concentration verified accurately against the published OSHA 1019 method.


When decontaminating


a room or enclosure, entry should be prohibited until the Occupational Exposure Limit (OEL), also known as Permissible Exposure Limit (PEL), has been reached so the area can then be safely released. The level is based on a time weighted average (TWA) over eight hours. The removal of hydrogen peroxide


from an enclosure is a logarithmic process, meaning that it takes a disproportionally long time to reduce from 2 to 1ppm compared to earlier in the cycle, therefore inaccuracy of 0.5ppm can have a significant effect on the cycle length. To resolve this issue, Bioquell has created the capacity to calibrate accurately at 1ppm. The calibration instrument produces a highly accurate


stream of hydrogen peroxide vapour at 1ppm concentration with better than ±0.1ppm accuracy. However, this relates to the accuracy of the calibration system, unrelated to the accuracy or repeatability of the sensor itself. The calibration method is highly


automated to ensure accuracy and repeatability and checked against the OSHA method to ensuring on-going accuracy.


For more information visit www.bioquell.com


SMART MONITORING TECHNOLOGY FOR BIOPHARMA MARKET P


owder containment and aseptic transfer valve specialist, ChargePoint Technology, has advanced its smart monitoring solution, Verifi, to support the biopharma market. The intelligent monitoring platform


is used to monitor usage data for ChargePoint’s split butterfly valves (SBVs). By recording how many times the


valve has been used and monitoring its temperature, Verifi generates data that allows operators and health & safety teams to manage the maintenance of their containment solution. Ultimately, this helps to improve efficiency and safety within chemical and pharmaceutical manufacturing processes. Malcolm Cunningham at ChargePoint says: “Verifi gives manufacturers an automatic and reliable method of understanding the health status of their valves so that they can take preventative action. This in turn improves operational performance, productivity and helps to manage risk. “The response from


customers in the pharma market so far has been


excellent. Verifi is not only giving the user confidence in the operational performance of SBV technology, but also the safety and quality teams peace of mind.” The software advancements now


available with the Verifi hub mean that it can connect directly onto the ChargePoint AseptiSafe valve unit, which is used to ensure sterility during aseptic processing. The data is then accessed from the device itself or remotely via an online dashboard. Cunningham adds: “We are thrilled to be


able to service the biopharma market. Given the growth in the biotech sector, extending the application of Verifi to this market is a natural next step for us. By adding technologies such as this to our portfolio, we are putting ChargePoint Technology at the forefront of overcoming sterile manufacturing challenges.”


For more information visit www.thechargepoint.com


www.scientistlive.com 21


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