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Nice response to my questions and good suggestions for moving forward.

Some of these sessions are too basic - this one had a good mix of basic and details. The tips are helpful. One comment: a little more discussion regarding the use of Detection in FMEAs would be useful since many do not advocate its use. Thanks,

I especially liked that the Q&A session after the webinar was long enough to not only address my own questions but also to learn from the questions from the other participants in the webinar.

Very thorough understanding of the history/progression of the guidances, and very helpful evaluation of current and potential directions. Excellent presentation skills, very engaging.



Analytical Instrument and Equipment Qualification in Quality Laboratories

Global CompliancePanel
Global CompliancePanel
Training Options
 Duration: 90 Minutes  
Recorded Access recorded version only for one participant; unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
Price: $295.00
Global CompliancePanel
Global CompliancePanel
Customer Testimonials
Instructor Richard Poser
Product Id 600144

Overview: The analytical instruments and equipment used in GXP laboratories must be calibrated and qualified for use in regulated testing.

This includes quality control labs attached to cGMP facilities, GLP labs supporting animal toxicology studies and GCP labs supporting clinical trials. Additionally, labs supporting EPA studies are also regulated. This seminar will review the regulations that cover each environment and present simple and effective strategies for satisfying the requirements. The impact of USP <1058> on analytical instrument qualification will be reviewed and the newest regulation will be presented in a simple and understandable way. The interaction of calibration, qualification, method validation and equipment maintenance on laboratory compliance and data quality will be discussed.

Why should you attend:
The analytical instruments and laboratory equipment are easy targets for inspectors looking to cite observations of non-compliance.  Are yours ready for the internal QA and external regulatory inspectors?

Areas Covered in the Session:

  • Regulatory requirements for analytical instrument qualification
  • Calibration and Metrology Programs
  • USP <1058>
  • ICH Q2
  • GXP
  • Equipment and Instruments - similarities and differences

Who Will Benefit:This webinar will provide valuable assistance to all regulated companies that need to validate their systems, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields and associated vendors such as contract research, manufacturing, testing and systems. The employees who will benefit include:

  • QC managers and personnel
  • QA managers and personnel
  • Information Technology managers and personnel
  • Validation specialists
  • Facility staff



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