Compliance4All, Online Event
2017-04-25
Overview: An analytical method is a process. The FDA process validation guidance applies to test methods, like all other processes in the pharmaceutical industry. Therefore, the laboratory or laboratories must demonstrate that a test method performs as intended through the method lifecycle.
Why should you Attend: Observations that test methods are inadequate or the firm does not have appropriate data that demonstrates the method performs as intended rank high on the list of observations in the laboratory.
Areas Covered in the Session: FDA System Based Inspection Guidance Laboratory Control System Most common observations in the laboratory Warning letter observations and analysis
Who Will Benefit: Quality Control Manager Supervisors Analysis and Microbiologists
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
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