When: |
25 Apr through 25 Apr 2017 | |
CFP Deadline: |
25 |
|
Where: |
Online Event | United States | |
Website URL: |
http://www.compliance4all.com/control/w_product/~product_id=501215LIVE?channel=mailer&camp=Webinar&AdGroup=brownwalker_Apr_2017_SEO | |
Sponsoring organization: |
Compliance4All | |
Categories: |
Medicine & Health - Medical-Speciality |
Keywords:
Event description:
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
Speaker Profile:
John (Jerry) Lanese is an independent consultant with a focus on Quality Systems and the components of an effective Quality System. He received a BA and MS from Middlebury College and...
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Posting date:
01 March 2017 | 130 views
Placement:
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