Auditing Analytical Laboratories for FDA Compliance

MessageThis Webinar is over
Date Jul 10, 2018
Time 10:00 AM to 11:30 AM
Cost $ 150.00
Online
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.

Areas Covered in the Session:
GMP Regulations that Apply to Analytical Laboratories
Reviewing Documentation
Advance Preparation for the Audit
Auditing Styles and Structures

Who Will Benefit:
Supervisors and Analysts in Contract Testing Laboratories
Personnel Responsible for Selecting Contract Testing Laboratories
Consultants

Speaker Profile:
Steven S. Kuwahara , Ph.D. is the founder and Principal of GXP BioTechnology LLC, a consulting firm that works in the areas covered by the GLP and GMP of drugs, biologics, and nutraceuticals. Steve has over 30 years of experience in supervising quality control laboratories, including an animal testing facility, and in performing GLP and GMP audits of internal and external testing laboratories.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

 


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