Equipment Calibration, Maintenance, and Validation: What Auditors Look for in a Controlled Process (Medical Devices)

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Jun 20, 2011 End Date/Time: Jun 20, 2011
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Why You Should Attend:
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 Seminar:

- Equipment Validation: Installation - Qualification, Operation Qualification, and - - Performance Qualification.
- Equipment Calibration Requirements.
- 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.
- Equipment Preventive Maintenance Requirements.
- Use of Calibration Standards to Save Cost.
- Remedial Action for Out-of-Calibration Equipment.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel involved in process development or equipment calibration/maintenance:

- R&D management
- Engineering management
- Production management
- Production engineers
- R&D engineers

NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.


Online Event
2600 E. Bayshore Road
Palo Alto
United States