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From IBC Asia (S) Pte Ltd
Auditing Clinical Trials for GCP Compliance 5-6 December 2011 Shanghai
...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, Investigators, Study Coordinators and Trial Center Managers who want to learn how to prepare for FDA and sponsor audits and to improve the quality of their research
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