← Clinical Data Services
Pharmacovigilance &
Postmarket Surveillance
Patients come first. Stay on top of safety with better surveillance.
Veranex can help you monitor your projects within a robust safety system and ensure consistent communication and pharmacovigilance writing with safety experts. Our team of 40+ experts works with your team to create a well-designed safety management plan (SMP) and prepare all applicable reports for drugs, biologics, and devices.
A Better Approach
What differentiates us from other service providers is the insight and all-around expertise we bring to our company.
We have a significant presence in India and two decades of experience implementing industry leading platforms enabling biopharmaceutical companies to better tackle their PV needs. We provide efficiency at a competitive cost while maintaining the highest standard in terms of quality and compliance.
Everything in One Place
With our in-house tracking and visualization tools, we manage deliverables leveraging prioritization, quality, and compliance.
We are a global company with multinational strategic locations, providing regulatory expertise across global markets:
- USA, Europe, & India (Bangalore, Hyderabad, Chennai, and Kolkata)
Our services include clinical development through postmarketing studies, with a host of integrated service offerings:
- Pharmacovigilance with clinical data management, medical writing and publishing, statistical programming and biostatics, data visualization, and functional sourcing
Our Pharmacovigilance/Device Vigilance Services Include:
- Case processing (clinical and postmarketing)
- Aggregate reports
- Literature screening
- Signal detection
- QPPV services
- Safety database hosting
- All other documentational logistics
- Global PV audits