Who uses QUOSA?
Pharmacovigilance and drug safety professionals
You need to screen scientific literature and triage for adverse events related to your products so that they can be promptly reported for regulatory compliance. With QUOSA, you can efficiently monitor safety-related literature and establish a product literature database so you can organize and store relevant articles for compliance reports, including PSURs, ICSRs and more.
Medical affairs and medical science liaisons
You need direct access to the latest literature so you can rapidly respond to client inquiries from anywhere. Access our central repository from your PC, Mac or iPad and find information quickly and easily – all in one place.
Medical device companies
You need to monitor scientific literature for mentions related to your products for clinical evaluation reports, pre-market approval and adverse events reporting. With QUOSA you can track and download relevant mentions within full-text articles, review them from your central library and easily create compliance reports.