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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.



Auditing Analytical Laboratories for FDA Compliance

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 Steven S Kuwahara
Product Id 600160

Overview: Auditing analytical laboratories can be complex because of the preparation that is often required.

All of the GMP rules do not apply to the laboratory; while there may be additional requirements depending upon the type of testing that is being conducted. In many cases, the laboratory itself may not understand what regulations apply to the work that is being conducted. This presentation will discuss what advance preparation is needed on the part of the auditor, and discuss what the auditor should look for during the audit. Since documentation is often an issue, a discussion of documentation problems will be presented.

Areas Covered in the Session:

  • GMP regulations that apply to analytical laboratories.
  • Reviewing documentation
  • Advance preparation for the audit
  • Auditing styles and structures
  • Equipment and laboratory instrument qualification.
  • What to look for while doing a walk-through.
  • Other regulations and standards, including ISO 17025
  • Following through on the audit

Who Will Benefit:This webinar will be of benefit to company auditors who need to investigate the qualifications of contract testing laboratories and internal testing facilities. It will also be beneficial to workers in laboratories that will be audited or inspected by external parties. Personnel from companies that perform testing on small molecule drugs, biologicals, and nutraceuticals will benefit from knowing what standards are being applied to them.

The following specific types of workers will benefit from this webinar:

  • External and Internal Auditors
  • Supervisors and Analysts in Quality Control Laboratories and Quality Assurance groups.
  • Supervisors and Analysts in Contract Testing Laboratories
  • Personnel Responsible for Selecting Contract Testing Laboratories
  • Consultants



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