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From IBC Asia (S) Pte Ltd
Auditing Clinical Trials for GCP Compliance 5-6 December 2011 Shanghai
Scheduled on 5-6 December 2011 a Shanghai, PR China. This 2-day course has been specifically designed for Clinical Quality Assurance Professionals who audit the quality of clinical trials, Clinical Research Associates (CRAs) and Managers, Project Leaders, and Medical Monitors who want to enhance their effectiveness, Regulatory Affairs Professionals responsible for GCP regulatory compliance,
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