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Conference Directory
Calibration and Qualification in Analytical Laboratories
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Venue Name: Online Event
Country: United States of America
City: Palo Alto
State: CA
Number of Attendees: Unknown
Webinar or Virtual Event: No
Keywords: Pharmaceutical development and quality control laboratories,Food, environmental, clinical and chemical testing laboratories,Suppliers of reference material,Contract laboratories,QA managers and personnel ,Analysts and lab managers,Validation specialists,Training departments,Documentation department,Consultants.
Start Date of Conference:: 03-26-2010
End Date of Conference: 03-26-2010
Description of Conference: Why Should You Attend:
Laboratory equipment should be calibrated and/or qualified to demonstrate suitability for the intended use. Laboratory systems including equipment are amongst key targets of FDA inspections. They are considered high risk systems because they have a high impact on product quality. Despite the fact that equipment calibration and qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify, test and document.
Attend this Webinar to know What FDA and other regulations say about equipment calibration and qualification? , the differences between calibration and qualification. How to develop and equipment qualification master plan, how does USP chapter fit in to calibration, what to do in qualification phases DQ, IQ, OQ, PQ. Also our expert Dr. Ludwig Huber will explain how to qualify/calibrate existing equipments.
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Calibration and Qualification in Analytical Laboratories
