Who we are?

MS Pharm is a GVP-compliant pharmacovigilance provider from Prague, specialized in local and global medical literature monitoring.

Local literature monitoring across Europe, the CIS and beyond

MS Pharm was established in 2015 in Prague, Czech Republic. We are a certified GVP-compliant PV provider specialized in local literature monitoring across Europe, the CIS region, the Middle East, Africa, South and Southeast Asia and other regions, as well as in global literature monitoring. Our team includes over 75 native reviewers, mainly healthcare professionals such as physicians and pharmacists.

Quality management system

All processes at MS Pharm are covered by an implemented quality management system, including business continuity and disaster recovery, project management, backup and data archiving, regular staff training and key performance indicator monitoring. Our system eDrug is used as a tool for QMS purposes, ensuring an audit trail of all entries.

Meet our team or explore our services: Local Literature Monitoring, Global Literature Monitoring and Local Pharmacovigilance Support.

Want to know more? Contact us for details and request a trial period.