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Validation Under Good Laboratory Practices 2017 

When: Mon., Dec. 4, 10-11 a.m. 2017
Phone: 800-447-9407
Email: support@compliance4All.com
Price: $ 150.00
www.compliance4all.com/control/w_product/~product_id=501596LIVE?channel=clevescene_Dec_2017_SEO
Overview: How to include critical reagents comparison, selectivity experiments, assessment of stability, importance of communication between the development and the validation labs and accuracy of transfer documents. Why should you Attend: Any laboratory that supports products for sale or use in the United States must follow Good Laboratory Practices (GLP), a comprehensive system that guarantees validity of results. If you work in pharmaceuticals, chemicals and petrochemicals, and environmental analyses then you are mandated to be following GLP. Areas Covered in the Session: Method Validation The Criteria for a Method Statistical Requirements Maintaining Compliance
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