Ensuring safe and effective real-world use of your product
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 post-marketing 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
- Expedited adverse event reporting
- Regulatory intelligence
- Aggregate safety reports and benefit-risk profile
- Post-marketing safety surveillance and risk managment
- 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?
