World Med Research
Advanced Post-Marketing Surveillance & Pharmacovigilance Platform
Empowering pharmaceutical companies, healthcare professionals, and researchers with comprehensive safety monitoring and regulatory compliance solutions.
Research Study Types
Comprehensive platform supporting various research methodologies and regulatory requirements
Featured Studies
Post-Marketing Surveillance
Comprehensive monitoring of drug safety and efficacy after market approval, including adverse event tracking and periodic safety reviews.
Start Post-Marketing SurveillancePharmacovigilance
Detection, assessment, understanding, and prevention of adverse drug reactions and drug-related problems.
Start PharmacovigilancePost-Marketing Surveillance
Comprehensive monitoring of drug safety and efficacy after market approval, including adverse event tracking and periodi...
Learn MorePharmacovigilance
Detection, assessment, understanding, and prevention of adverse drug reactions and drug-related problems.
Learn MoreClinical Trials
Controlled studies to evaluate the safety and efficacy of new treatments in human subjects.
Learn MoreMeta-analyses
Statistical analysis combining results from multiple scientific studies to increase power and improve precision.
Learn MoreRetrospective Studies
Analysis of existing data to identify patterns, outcomes, and relationships in previously collected information.
Learn MoreCohort Studies
Observational studies following groups of individuals over time to assess exposure and outcome relationships.
Learn MoreCase-Control Studies
Comparative studies between cases with a specific condition and controls without the condition.
Learn MoreCross-sectional Studies
Snapshot analysis of a population at a specific point in time to assess prevalence and associations.
Learn MoreSystematic Reviews
Comprehensive synthesis of all available evidence on a specific research question using systematic methods.
Learn MoreRegulatory Studies
Research conducted to meet regulatory requirements and guidelines for drug approval and monitoring.
Learn MorePlatform Features
Advanced tools for comprehensive pharmacovigilance and research
Role-Based Access
Customized interfaces for physicians, brand managers, medical reps, patients, and researchers.
Real-time Analytics
Comprehensive dashboards with hierarchical data visibility and safety signal detection.
Regulatory Compliance
Built-in compliance with ICH GCP, FDA 21 CFR Part 11, and global pharmacovigilance standards.
Mobile Responsive
Optimized for all devices with seamless data entry and monitoring capabilities.
Safety Monitoring
Advanced adverse event tracking with severity assessment and automated reporting.
Secure Data Management
Enterprise-grade security with encrypted data storage and audit trails.
Ready to Transform Your Pharmacovigilance?
Join leading pharmaceutical companies and healthcare organizations in revolutionizing drug safety monitoring.