Short Abstract

To attend this webinar kindly call 1-646-216-8860 or email at marketing@biopractice.com

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 product that meets its specifications. However, there are ways to validate equipment already in use!

This webinar will discuss Equipment Calibration Requirements, Preventive Maintenance Requirements, when to use Calibration when to use Maintenance, what is Remedial Action for Out-of-Calibration Equipment, how to use of Calibration Standards to Save Cost.

Areas Covered in the Webinar:

• Equipment Validation: Installation Qualification, Operation Qualification, and Performance Qualification..
• Equipment Preventive Maintenance Requirements.
• Calibration vs. Maintenance: When to use Which One?
• Remedial Action for Out-of-Calibration Equipment.
• Use of Calibration Standards to Save Cost.
• Equipment Calibration Requirements: Scheduling, Use of External Services, and Documentation.