Pharmacovigilance
Safeguarding Patients. Strengthening Confidence
OVERVIEW
Solutions Across the Product Lifecycle
- Patient safety is our top priority.
- Global regulatory compliance
- Risk identification and minimization
- Data-driven decision making
- Quality, accuracy and timelines
OUR PHARMACOVIGILANCE SERVICES
End-to-End PV Support
Safety Case Processing
Intake, triage, case processing and close monitoring for safe and accurate data collection.
Literature Surveillance
Comprehensive literature screening and ongoing surveillance for safety signals.
Signal Detection & Management
Signal identification, evaluation, prioritization, and continuous monitoring.
PSUR Development & Maintenance
Development and maintenance of periodic safety update reports.
PV System Management
Quality, maintenance and audit of PV systems and processes.
Regulatory Reporting
Submission of IC SR, PSUR forms, and other reports.
OUR PV PROCESS
A Structured Approach Measurable Results.
Intake
Receive safety data from multiple sources.
Assess
Medical evaluation and data verification.
Analyze
Signal detection and risk assessment.
Act
Regulatory reporting and risk minimization.
Monitor
Continuous monitoring and improvement.
WHY CHOOSE Qualitatva
Your Trusted Pharmacovigilance Partner
20+ Years of Experience
Deep expertise in life sciences and regulatory compliance.
PV Experts
Dedicated PV professionals with hands-on PV and regulatory experience.
Global Compliance
Aligned with global PV guidelines and regulatory reporting standards.
Quality & Accuracy
Focused on quality, accuracy and timely deliverables.
Technology Driven
Advanced tools and technology used for better insights.
Client Focused
Customised PV solutions tailored to your business needs.
Committed to Patient Safety. Dedicated to Your Success.
Partner with Qualitatva for reliable pharmacovigilance solutions that ensure compliance, reduce risk and protect patients.