A central monitoring system provides a solution for automated continuous monitoring. It will enable your facility to have fast, standardized responses to alarms and efficient, electronic reporting capabilities, adding a superior level of protection for your irreplaceable products.
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Processing excursions and conducting quality investigations use extensive resources. Ineffective data handling processes can take so much time, some companies never get to value add activities such as trending cold chain data. Today, with the cost-effective technology available, that should never be the case. So why isn’t every pharmaceutical company using a state-of-the-art data monitoring system with advanced reporting and analytics capabilities?
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Environmental / temperature monitoring plays a vital role in the manufacturing (cGMP) and healthcare (JCAHO, CAP, USP 797) markets. In the event of a temperature excursion, do you know if your product is still acceptable? Would you lose valuable product or days worth of testing time?
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If your facility is growing or has come under the purview of GxP regulatory review, you know that data is the critical for healthcare facilities like hospitals to comply with JCAHO or Pharma to comply with FDA 21 CFR 11. Regulators want to see evidence that demonstrates maintenance of correct environmental conditions for healthcare related materials and products being stored in a facility.
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