Maintenance and Calibration of Equipment

Instructor: Michelle Sceppa
Product ID: 701188
  • Duration: 60 Min

recorded version

1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542


Read Frequently Asked Questions

This Pharmaceutical compliance training will provide instruction on how to establish and maintain a Maintenance & Calibration program for pharmaceutical instrumentation & equipment.

It is a Regulatory Requirement to establish a program for the preventive maintenance and calibration requirements for equipment and instrumentation used for characterization, testing and/or release of pharmaceutical & biotechnology products.

Areas Covered in the seminar:

  • Definitions.
  • Requirements of the systems being maintained and calibrated.
  • Intervals for maintenance and calibration.
  • Maintenance and calibration procedures.
  • Remedial action in the event of a failure.
  • Management of the metrology program - equipment calibration tracking and management software.

Who will benefit:
This webinar will provide instruction on how to establish and maintain a Maintainance & Calibration program for pharmaceutical instrumentaition & equipment

  • Managers
  • Supervisors and Associates in the Pharamceutical Industry that have daily responsibilities in Quality Assurance
  • Quality Control, Compliance and Facilities & Engineering

Instructor Profile:
Michelle Sceppa, is the Principal at MSceppa Consulting, an establish Consulting firm and is in its 12thth year in the Industry that specializes in quality systems for Pharmaceutical and Biotechnology interests. MSceppa Consulting has implemented and managed Preclinical, Clinical, and Manufacturing Quality Assurance Programs for numerous clients. As the lead auditor, MSceppa Consulting has conducted and managed more than 400 internal and external vendor audits for Drug and Biologic firms in the US and Europe. MSceppa Consulting is knowledgeable in the details of compliance with all U.S. Federal Regulations-Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP) for Drugs, Biologics and Medical Devices.

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