Description
Key Features and Benefits
- Automated Compliance Management – Simplifies regulatory compliance by integrating audits, inspections, and risk management.
- Supplier Quality Management – Centralized platform for managing supplier risk, quality performance, and compliance.
- Document Control & Training Management – Tracks, approves, and maintains training and compliance records efficiently.
- CAPA & Non-Conformance Handling – Supports structured workflows to track corrective and preventive actions.
- Audit & Inspection Management – Helps organizations remain audit-ready with automated scheduling and reporting.
- Postmarket Surveillance – Reduces manual efforts in monitoring product safety and compliance post-launch.
- Integrated Analytics & Dashboards – Offers real-time insights into quality and regulatory performance.
Key Differentiators
- Life Sciences Focus – Designed specifically for pharmaceutical, biotechnology, and medical device companies.
- Connected Intelligence Approach – Uses IQVIA’s analytics capabilities to enhance regulatory compliance and operational efficiency.
- End-to-End Process Automation – Reduces manual compliance tasks and speeds up regulatory response times.
- Scalability – Suitable for organizations of varying sizes, from startups to large enterprises.
