#pvcompliance

Delayed literature review can increase pharmacovigilance compliance risk when critical evidence is missed, safety assessments are slowed, and regulatory timelines become harder to meet. In PV workflows, timely literature review is essential for identifying relevant safety information and supporting patient safety decisions.

As global health authorities tighten pharmacovigilance expectations, companies need reliable systems to ensure safety, compliance, and continuity. Our PSMF and Global QPPV Solutions are designed to provide complete transparency and control over your drug safety operations.

Through a meticulously structured PSMF, we capture essential details about processes, systems, and responsibilities, while our Global QPPV ensures 24/7 oversight, issue escalation, and strategic guidance. Together, these elements create a robust framework for managing safety data and meeting local as well as international regulations.