🎤  HitendraKumar Shah      |  📅  October 27, 2022   |  🕒  11 AM Eastern Time US


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.

Areas Covered in the Session :

  • Definitions and Regulatory Expectations
  • Preventive Maintenance Requirements
  • Equipment Calibration Requirements
  • Calibration vs. Maintenance: When to use Which One?
  • Intervals for maintenance and calibration.
  • Maintenance and calibration procedures.
  • Remedial Action for Out-of-Calibration Equipment
  • Use of Calibration Standards for Efficiency and Accuracy

Who Should Attend:

  • Quality Departments
  • Engineering Departments
  • Research and Development Departments
  • Production Departments
  • Manufacturing Departments
  • Validation Departments
  • Operations Departments
  • Design Engineers
  • Reliability Engineers
  • Calibration Technicians
  • Maintenance Personnel

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