URAS PV supports pharmaceutical companies through two connected service lines: pharmacovigilance and drug registration in global, CIS, EAEU and Turkish markets.
End-to-end pharmacovigilance for marketing authorisation holders: qualified persons, PV system documentation, case processing, signal management, literature monitoring and audits.
Regulatory affairs support across the CIS and Eurasian region: new registrations, registration models, renewals, variations, price registration and trademarks.
Our expertise includes Local QPPV and EAEU QPPV services, Individual Case Safety Report (ICSR) management, local literature monitoring, pharmacovigilance system documentation, and regulatory support.
Pharmacovigilance across the CIS and TürkiyeTalk to our team and let us design a tailored solution for you.
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