<p>Spontaneous Reports<br/> Time Frames For Regulatory Reporting<br/>MedDRA<br/>WHO Drug Dictionary<br/> Action Taken DC and RC<br/>Causality Assessment<br/>Unblinding @ SUSAR<br/>Post Treatment and Pre-Treatment Study<br/>Eudravigilance.<br/> EMEA - GVP VI<br/> FDA: Adjudication and Advisory Panel<br/> Vioxx Mediator; Thalidomide<br/>Signal Detection<br/> ARGUS<br/>Narrative Writing – Rules & Format .<br/> Important Medical Event List<br/> Serious vs Non-Serious: Thumb Rules</p>
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