Post-marketing pharmacovigilance is a critical component of the drug development lifecycle, ensuring safe and effective use of marketed therapies in the real world.
Allucent provides global post-marketing pharmacovigilance (PV) solutions that integrate expertise in pharmacovigilance, medical, regulatory affairs, clinical operations, and quality assurance, leveraging technology-driven efficiencies to minimize manual effort and reduce costs.
From PV system set-up and lifecycle maintenance, Allucent delivers operational excellence through highly agile PV operations, comprehensive safety surveillance and risk management solutions, global QPPV and local affiliate services, and technical PV consulting including global PV audit strategy development and execution.
Post-Marketing Pharmacovigilance Solutions
- PV planning and strategy development
- PV system and global safety database set-up and management
- Adverse event management and expedited reporting
- Regulatory intelligence
- Aggregate safety reports and benefit-risk profile
- Safety surveillance and risk management
- Qualified Person responsible for PV and PV System Master File
- Local contact person for PV
- Global and Local Literature screening
- GVP audits and inspection readiness
- SDEA/PVA management
- Consultancy Services
Global Safety Database & Legacy Data Migration
Do you have safety data in multiple systems that needs migrating to a global safety database?
Post-Marketing Pharmacovigilance Technology
Interested in using technology to automate processes and reduce manual effort?
Global Pharmacovigilance Obligations
Need support with local PV obligations and intelligence globally?
