Analytical Method Validation in FDA process - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501215LIVE?channel=mailer&camp=Webinar&A |
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Category pharmaceutical, Medical device compliance webinar, medical device calibration requirements, pharmaceutical manufacturing, largest pharmaceutical companies, Fda compliance guidelines, Analytical Method Validation, method validation
Deadline: April 24, 2017 | Date: April 25, 2017
Venue/Country: Fremont, U.S.A
Updated: 2017-02-24 19:02:13 (GMT+9)
Call For Papers - CFP
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 GuidanceLaboratory Control SystemMost common observations in the laboratoryWarning letter observations and analysisWho Will Benefit:Quality Control ManagerSupervisorsAnalysis and MicrobiologistsSpeaker 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 a Ph.D. in Analytical Chemistry from the University of Michigan and began his career teaching Analytical Chemistry in a small liberal arts college. Dr. Lanese moved from the academic environment to the pharmaceutical industry where he has managed Analytical Research, Quality Control and Quality Assurance functions.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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