Events Tagged "clinical trials"

Meeting FDA Requirements for Clinical Trials

This 90-minute webinar will provide an overview of regulatory management for clinical trials. It will discuss key regulatory aspects of a clinical project such as clinical protocol management.

Medical Device Adverse Event Reporting

This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada.

Risk Analysis Techniques in Clinical Trials

This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.

Detection and Escalation in Clinical Trial Setting

This webinar on issue detection and escalation in clinical trial settings will review the responsibilities of sponsors, investigators, IRB in clinical trial setting to maintain compliance.

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