Course - Los Angeles, CA, United States
This two-day course is designed for all persons who work in, supervise, or are involved in the management of pharmaceutical, biopharmaceutical, and biologics Quality Control Laboratories. The course will also be of benefit to entry-level Quality Assurance professionals and others who audit QC Labs, or whose responsibilities include insuring lab regulatory compliance. This course will also provide participants with an understanding of how to effectively handle out-of-specification results, deviations, laboratory investigations and Corrective and Preventive Actions.
This course is intended to give participants a thorough overview and practical understanding of Current Good Manufacturing Practices for laboratory compliance including:
General requirements for design and construction of analytical laboratories
Calibration and Qualification of instrumentation and equipment
Documentation, records-keeping and change control
Management of reagents, test solutions and reference standards
Personnel development and training
(Courtesy of http://www.cfpie.com/)
Thu, Aug 30, 2012 - Fri, Aug 31, 2012
The Hilton Los Angeles Airport (LAX)
5711 West Century Blvd., Los Angeles, CA 90045, United States
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