Verius Ltd acquired by ProductLife Group

Verius Limited offers a complete range of pharmacovigilance and medical monitoring services, with a unique ability to tailor our services directly to your needs. We have global capabilities and work within all applicable regulatory and international requirements. In today's environment there is an ever increasing focus on the safety of new products... . Verius Limited can provide services ranging from a basic Pharmacovigilance service through to a sophisticated system encompassing data capture, medical review, narrative writing and electronic SUSAR reporting. Verius can offer analyses of similar events, with reports to regulatory authorities and the EMEA when necessary. With our industry standard fully validated safety database system which is E2B and 21 CFR Part 11 compliant, we can produce ICSRs, monthly line-listings, annual safety reports and periodic safety update reports. Starting with CRF/protocol review and investigator training through medical monitoring, safety database completion and expedited reporting to the end of study reports and case narratives, we are able to provide the pharmacovigilance expertise needed for clinical trials at every stage. Our post-marketing services include the provision of a qualified person for Pharmacovigilance (QP PV), signal detection, literature searches, and risk management planning either on a stand alone basis or as part of the regular safety services. With our wide experience and knowledge we offer the complete solution. We have the required skills to monitor the safety of your product from the clinical stage to marketing approval and beyond, covering clinical trials, post marketing studies, spontaneous reports and literature searches.Read More