IQVIA MedTech offers proactive post-market surveillance (PMS) solutions to help manufacturers manage recalls, regulatory reporting, and adverse event tracking. The fact sheet emphasizes a shift from reactive to predictive approaches, leveraging technology, analytics, and scalable resources. Services include complaint handling, FDA eMDR submissions, vigilance evaluations, recall coordination, and remediation support. By integrating regulatory expertise with cloud-based systems and real-time reporting, IQVIA enables earlier detection of issues, ensures compliance with global requirements, and reduces downstream risks. These comprehensive PMS services minimize business disruption and enhance patient safety.

Join for free to read