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Date	Description
12/05/2008	Medifest 2008: Vantage Trade Fairs (P) Limited
12/05/2008	2nd Annual World Congress of Gene 2008: BIT Life Sciences
12/05/2008	National and International Regulatory, Legal, and Ethical Environment in the Bioscience Industry: Oregon Graduate Institute School of Science & Engineering
12/06/2008	National and International Regulatory, Legal, and Ethical Environment in the Bioscience Industry: Oregon Graduate Institute School of Science & Engineering
12/07/2008	Annual Forum of the Antibody Engineering: IBC Life Sciences
12/07/2008	Antibody Engineering: IBC Life Sciences
12/08/2008	BMD Summit: IBC Life Sciences
12/08/2008	Intelligent Leadership training for scie: Cambridge Healthtech Institute
12/09/2008	Quality System Audits: Lessons Learned in Medical Device Risk Management: Complianceonline
12/09/2008	Antibody Therapeutics: IBC Life Sciences
12/10/2008	Integrating Risk Management with the Quality System: Complianceonline
12/10/2008	Deviations and Process Failures within a CAPA program: Complianceonline
12/10/2008	Overview of how 21 CFR Part 11 helps ensure data integrity and subject safety in clinical research: Complianceonline
12/10/2008	Southwest Virginia Science Forum: VaBIO
12/11/2008	How to Avoid an FDA Warning Letter with a Strong CAPA Program: Complianceonline
12/13/2008	48th ASCB Annual Meeting: American Society for Cell Biology
12/16/2008	Clearing up Roles and Responsibilities in the GLPs: Complianceonline
12/17/2008	The Art and Science of Study Participant: Complianceonline
12/17/2008	Maintaining a Sustainable and Compliant Design Validation System and Using FMEA for Device Manufacturers: Complianceonline
01/06/2009	CHI’S High Content Analysis Content 2009: Cambridge Healthtech Institute

(next 20 events)

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