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Laboratory Have an Instrument Calibration Program -2020
Date
Oct 12, 2021 - 10:00 AM
Link to Website
Organizer
Netzealous LLC DBA - Compliance4All
Venue
online
Location
Netzealous LLC DBA - Compliance4All,
Fremont,
CA,
US,
ZIP: 94539
Phone: 18004479407
Ticket Price: $ 150.00
Overview:
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
classifications.
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
tolerance.
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
Email: [email protected]
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
classifications.
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
tolerance.
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
Email: [email protected]
Event Categories
Keywords: HealthCare , program , laborator