Integrated Solutions to Drive Proactive Post-Market Surveillance

The medical device vigilance process requires you to collect, analyze, and report adverse events and product malfunctions. It can be challenging to know what is reportable and by when you need to notify the regulatory bodies. This is particularly true as the volume of adverse events communicated via social media, real world evidence, and other proactive sources grows in significance.

IQVIA MedTech has the experience, vision, and technologies to support manufacturers and identify the most relevant PMS solutions for their organization.

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