Calibration and Assuring Accurate Measurements

Assuring accurate measurements is important when establishing specifications during product design and development, during process validation and for assuring product performance while testing for lot release.

Assuring accurate measurements accounts for a significant amount of time and resources in assuring product conformance. This talk will shed light on the issues for maintaining a successful measurement and calibration program.

Participants should have some previous experience with calibration and measurement systems, but otherwise, this talk is applicable to all levels, especially management, as it covers underlying principles in a simplified format. (These are often overlooked in other basic and intermediate how to courses).

Areas Covered in the Session :
General data integrity and calibration concepts
How to instill meta-data awareness in those doing measurements and/or are responsible for maintaining the calibration/measurement programs.
Documentation requirements for calibrations and test results and investigating out of tolerance findings to prevent recurrence.

Who Will Benefit:
This discussion will provide individuals with a better understanding of data integrity and measurement variation sources and should be of interest to:
Technical Supervisors
All professionals responsible for data accuracy in any organization

Antony J. DeMarinis

Tony DeMarinis has BS degrees in Biology & Microbiology and a MS in Quality Management. He is currently an independent Consultant specializing in Sterilization, Quality Systems, Auditing, and other Quality Management issues in the medical device and pharmaceutical industries. Previously, Tony was Director of QA/RA at Tunstall Americas for electronic monitoring devices, Quality Manager at Sealed Air for medical packaging, Quality Systems Manager at Davol for implants and surgical devices, Director of Quality Assurance at Scott Laboratories for in-vitro diagnostics and Sr. Microbiologist at the National Cancer Institute.

He is recognized as a Fellow by the American Society for Quality, and he is a Certified Quality Auditor, BioMedical Auditor, Six Sigma Black Belt, Pharmaceutical GMP Professional and Manager for Quality and Organizational Excellence. He also teaches the refresher courses for the CQA and CMQ/OE certification programs through the local ASQ sections. Tony has over 25 years’ experience using quality management techniques and value added auditing including the use of Failure Investigation and Root Cause Analysis to improve processes and products.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance