Masterclass: Reviewing Informed Consent Forms (ICFs) for Compliance and Ethical Considerations
Register Informed Consent is the cornerstone of ethical clinical research, ensuring that participants fully understand their […]
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Masterclass: Ensuring Drug Accountability in Clinical Trials
Register Maintain Compliance and Data Integrity Through Effective Drug Management In clinical trials, drug accountability […]
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Masterclass: Performing Source Document Verification (SDV) and Risk-Based Monitoring
Register Are you an aspiring or early-career clinical research professional wanting to enhance your industry […]