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End-to-end services for high-quality safety and pharmacovigilance operations
Technology-driven solutions integrated into the pharmacovigilance landscape
PVConsult™
Optimise your PV operations through monitoring and use of technology by our SMEs.
PVTransition™
Come to rescue of your PV systems during service provider modifications or technology switch.
PVBridge™
Help our long-standing clients to develop in-house pharmacovigilance capacity.
PVIntegrate™
Streamline your PV systems and processes during expansion.
PVExpert™
Strengthen your negotiations with regulators, HTAs and external stakeholders.
Product expertise which enables efficiencies in PV operations
Innovative/Brand Products
Support the development of PV plans and risk minimization measures pre- and post-marketing.
Generics, Hybrids, Biosimilars
Methodical management of challenging PV agreements, signal detection, audits schedules & conduct and training.
Vaccines
Comprehensive PV management of seasonal vaccines ICSRs and systems to enable seamless end-to-end operations.
Devices and Combination Products
Our experts can advise you on your vigilance system, post-market surveillance and safety reporting.
Pediatric Medicines
Support tailored PV research in pediatrics and draw lessons from risk minimization of ARs in adult population.
Medicines for Older People
We adjust your RMPs cognizant that co-morbidities or side effects - specific to older patients - will shape PV activities.
Insights Hub
Trending Topics, Case Studies, Articles
Latest Case Study
PrimeVigilance’s Effective Approach to New Region Expansion
Uncover how PrimeVigilance navigated the complexities of expanding Medical Information (MI) services into Japan, establishing a strong foundation in a new and challenging market.
Published: 7 November, 2024
Webinars
Latest Webinar
The Regulatory Landscape of AI: The Current State and Future Trends
This session explores the critical role of regulatory compliance in AI development, deployment, and governance, highlighting strategies for balancing innovation with ethical and legal requirements. Join our expert speaker, Nikodem Latocha, as he provides actionable insights into navigating this dynamic landscape, ensuring your organization stays ahead of regulatory changes.
Published: 14 November, 2024
Duration: 40 Mins
News and Events
Events
Latest Article
Nikola Lazarevski (Associate Director, Medical Writing)
Stephan Examitzki (PV Project Director, Biosimilars and Generics)
Elena Alcaraz Garcia (Strategic Advisor, EU & UK QPPV)
Alessandro Di Ranno (