← 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