Clinical Pharmacovigilance

The documentation and analysis of the safety data us critical in clinical trials management. Our ICSR Specialists provide project management, subject matter expertise, and case processing services tailored to your needs. Our team pay complete attention to all case processing and quality review activities. We also provide postmarketing PV and thus it is easier for our client to transition from clinical to postmarketing services.

High-Quality Processing

We have an extensive experience in clinical PV services and specialize in providing ICSR processing in a fully compliant and validated safety database. We are regularly audited and ensure technological upgradation at regular intervals to stay ahead the curve. We pay close attention to any changes in the regulatory framework and adapt them quickly to the core regulatory reporting procedures.