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Laboratory Have an Instrument Calibration Program -2017

 
  August 09, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2017-10-10


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

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
 
 
Organized by: Event Manager
Invited Speakers:
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.
 
Deadline for Abstracts: 2017-10-09
 
Registration:
Full Details & Registration Link:
E-mail: support@compliance4All.com
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