Our Sponsors
FDA VALIDATION 2011 - Understanding and Implementing USP <1058>: Analytical Instrument Qualification
Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=700067?channel=ourglocal |
Edit Freely
Category FDA Validation,Food Safety,conference,event,Webinar
Deadline: March 22, 2011 | Date: March 22, 2011
Venue/Country: Palo Alto, U.S.A
Updated: 2011-02-02 18:52:55 (GMT+9)
Call For Papers - CFP
Why Should You Attend:Analytical instruments should be qualified to demonstrate suitability for the intended use. Companies are unsure on what exactly to qualify or re-qualify, test and document. The main reason is that unlike for analytical methods there was no clear standard with details for equipment qualification. This has changed. The USP has developed a chapter that provides a framework for analytical instrument qualification (AIQ).This USP <1058> webinar will give a good understanding of current and future FDA requirements and the USP framework. It also will provide detailed steps, examples and tools for cost-effective implementation.NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.