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Minimizing calibration risk in complex biotech environments

by Blue Mountain Quality Resources Inc.

As part of the regulatory environment created by the U.S. Food and Drug Administration, a life science company must prove that its assets are properly managed, including instrument and equipment calibration, maintenance and validation. This white paper by Blue Mountain Quality Resources Inc. explores minimizing calibration risk in complex biotech environments. For many biotech organizations outsourcing all or part of their calibration system and processes is the solution. This paper explains several unique characteristics of biotech organizations that complicate the management of calibration and discusses minimizing risk using a Calibration Master Plan.

Published: 2005
Format: PDF
Length: 7 pages
Type: White paper
Language: English
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