Drug Safety and Pharmacovigilance

Effective processing of clinical trial safety data is imperative to the successful conduct of a clinical trial or guarantee post-marketing safety. Neox offers effective management of clinical trial and post-marketing adverse events from case assessment through to expedited. Neox will take care of all of your requirements for case processing, expedited reporting, periodic safety update reports (PSURs), literature screening and safety signal detection and review. If needed we provide and run your entire pharmacovigilance operation. See below areas of pharmacovigilance where Neox provides high quality services: