Less Pain for Adverse Events

New CDISC guidelines streamline AE and SAE reporting By Kathryn E. Vinson, MS, CCRC, with input from LeeAnn Phipps, PV Manager, DZS Clinical Services Nobody wants adverse events (AEs), much less serious adverse events (SAEs) to happen. The reasons that we in clinical research despise AEs are multitude, not the least of which is that […]