“Eupry saves us over five hundred Doing the job several hours yearly, permitting us to employ that point for other important tasks. Automatic temperature monitoring allows us to unwind outside of Operating hrs (…).
Even so the simplicity of your temperature compliance Answer can make it don't just straightforward to implement and use, In addition, it makes it straightforward to grasp why the new route is actually the only real appropriate approach to do issues.
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One-simply click reporting, easy access to all the information you require, and digital storage of Your temperature information – from calibration certificates to temperature records and deviations. With every thing available, it is simple to discover the knowledge that issues most.
Eupry Aps presented (…) documentation to conclude that methods and successful controls to make certain compliance are in position and well-working as meant in all vital places/procedures (…)
From customers to colleagues: Rocking the boat and obtaining Absolutely everyone onboard with new ways of Functioning may be tricky.
Own details is managed As outlined by CCPA and GDPR expectations, delivering an extra layer of assurance for your personal facts's safety. Given the stringent regulatory landscape during the pharmaceutical sector, the need for compliant facts handling is especially higher, Which is the reason our services is engineered to fulfill the highest criteria, supporting your compliance.
The ISO-accredited Resolution have a peek at this web-site is ideal for all types of cargo – such as very controlled pharmaceutical products and solutions.
“The response instances and availability from Eupry ended up pretty remarkable. We now have repeatedly been in contact with each other each individual move of the best way.
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1-simply click reporting, easy access to all the information you will need, and electronic storage of Your temperature knowledge – from calibration certificates to temperature records and deviations. With anything accessible, it is easy to find the knowledge that issues most.
With many mappings underneath our belt, we know greatest methods and the way to transform the ever-modifying regulations and guidelines of your pharma earth into action.
While using the audit trail, it is straightforward to procedure the non-conformity or to prove that anything was in established parameters, so we could possess the report Completely ready in compliance with GMP demands.“
“Specifically convenient would be the automatic calibration Source procedure where by external calibrated sensors are replaced with new calibrated ones mechanically,“