Preventive Maintenance and Calibrations – Regulatory Expectations and Best Practices

Description:

FDA and EU regulations require that firms have a program for the calibration and maintenance of test and measurement equipment. The program must include intervals, scheduling, specific procedures, limits of accuracy/precision, and remedial action in the event that the equipment does not meet established requirements. Prior to use, however, this equipment must be validated to make sure it produces a product that meets its specifications. There are ways, though, to validate equipment already in use.

This webinar will provide instruction on how to establish and maintain a Maintenance & Calibration program for medical device and pharmaceutical instrumentation & equipment.