Pharmacovigilance and Drug Safety Software

Clinical Research, Drug Safety and Pharmacovigilance

Training on entering event information in Argus Safety database - SlideServe

QPS Selects Oracle Argus Safety Database to Enhance Pharmacovigilance in Clinical Trials

 Signals of adverse drug reactions (ADR) can be based on different study designs, including clinical trials, observational studies, meta-analyses, and case reports. Daniele Sartori sat down in the Research Corner to shine a light on the evidence base and features of ADR reports. Watch the film below Curious about the topic? Access the report for further reading  doi.org/10.1007/s40264-022-01258-0 #pharmacovigilance #PatientSafety | Uppsala Monitoring Centre | Facebook

1.7K views · 18 reactions |  Adverse event reports typically contain...