Comprehensive Clinical Research Services
From Strategy to Submission—We Deliver with Precision
ClinVira provides end-to-end clinical development services tailored to the unique needs of sponsors across the globe. Our team of experts delivers strategic guidance, operational excellence, and regulatory compliance to accelerate drug development—ensuring every trial is efficient, ethical, and impactful.
End-to-End Solutions for Smarter Drug Development
From First-in-Human to Post-Market Safety—We’ve Got You Covered
ClinVira offers a full spectrum of services across clinical research, pharmacovigilance, and regulatory compliance. Whether you’re designing a complex oncology trial or scaling post-marketing safety globally, our unified approach ensures precision, speed, and transparency.
Clinical Trial Management
Accelerate every phase of your clinical research—from feasibility to final report—using our digital-first operations, deep therapeutic expertise, and real-time study oversight.
Pharmacovigilance & Drug Safety
Ensure global safety compliance through our AI-enhanced pharmacovigilance services, including case processing, signal detection, QPPV support, and multilingual medical information.
Regulatory & GxP Compliance
Stay audit-ready with our proactive regulatory support—covering GCP, GMP, GLP, and CSV audits, submission guidance, and risk-based quality oversight.
Why ClinVira
Built for Speed, Designed for Compliance, Driven by Innovation
Digital-First Clinical Operations
Patient-Centric Engagement
Integrated Safety & Regulatory Services
Global Reach with Local Insight
Real Stories. Real Results.
Trusted by Innovators Around the World
“ClinVira accelerated our oncology trial by months. Their digital-first processes, proactive site engagement, and true partnership mindset made all the difference.”
“We switched to ClinVira mid-trial due to delays with another CRO—and never looked back. Their project team was transparent, fast, and deeply knowledgeable.”
“ClinVira’s pharmacovigilance team helped us meet global compliance across 25 countries. Their safety intelligence platform and QPPV support are top-notch.”