Laboratory Have an Instrument Calibration Program -2017

This web seminar builds on the terminology found in 21CFR160(b)(4) and

introduces terminology and concepts not found in the regulation, but

necessary for an effective calibration program, such as instrument

Why should you Attend:
In this webinar we will discuss instrument classification, getting the instrument

into the calibration program, removing the instrument from the calibration

program, instrument classification, limits of accuracy and precision and

remedial actions in the event that an instrument is found to be out of


Areas Covered in the Session:
The Regulatory and Technical requirements for calibration
What Should be Included in a Calibration Program
The Importance of a data-based Calibration Interval and Limits of Accuracy

and Precision
The Impact of Measurement Uncertainty when Establishing Limits of Accuracy

The Classification of Test Instruments

Who Will Benefit:
Laboratory Managers
Laboratory Supervisors
Laboratory Analysts
Quality Assurance Managers
Quality Assurance Record Reviewers

Speaker Profile:
John (Jerry) Lanese is an independent consultant with a focus on Quality

Systems and the components of an effective Quality System. He received a BA

and MS from Middlebury College and a Ph.D. in Analytical Chemistry from the

University of Michigan and began his career teaching Analytical Chemistry in a

small liberal arts college. Dr. Lanese moved from the academic environment to

the pharmaceutical industry where he has managed Analytical Research,

Quality Control and Quality Assurance functions.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
At a Glance
When 10 October 2017
Where Fremont, CA, United States
Organizer Netzealous LLC DBA - Compliance4All
Event Type conference
Official Website
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Added by Compliance4all
Added on 09 August 2017
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