Incubator Claibration
Due to heightened quality requirements from regulatory bodies such as the NYS DOH, from customers and from internal quality assurance
guidelines, equipment calibration is more important than ever. As an NYS DOH-regulated company, you may be audited for your compliance with
NYS-DOH regulatory requirements – either GLP (Good Laboratory Practices) or GMP (Good Manufacturing Practices). The NYS-DOH requires
that the display accuracy of all instruments that have an effect on the quality of your product be verified (calibrated) over a specified interval of time.
We have successfully helped our clients comply with regulations and pass NYC DOH, AAAHC, AAAASF, CAP, and The Joint Commission Surveys.
We can also help you to achieve high standards that you are striving for.
ACE Medical Equipment provides on-site centrifuge calibration using high accuracy equipment. Our Ultra-Class calibration tools uphold
unsurpassed industry leading accuracy. This level of accuracy ensures precise results even for customers who maintain the most stringent
process tolerances.
Upon completion of calibration, ACE Medical technicians will leave you with detailed calibration certificates, with information on
as-found data, as-left data, test point deviations, instrument tolerance and instrument operating range.
Temperature mapping of Incubators
Incubators allocated for the storage and handling of products with a specified labelled storage temperature require mapping. A
mapping study establishes the temperature distribution within the zone being mapped and it locates hot and cold spots. The collected data
provides an essential source of information to ensure that all products are correctly stored within their labelled temperature range(s).
Mapping may also be used to identify zones where remedial action needs to be taken; for example by altering existing air distribution to
eliminate hot and cold spots. Mapping takes 24 hours to create an accurate chart of temperatures in the incubators.