Postmarket Surveillance

/ˈpoʊstˌmɑrkɪt sɜrˈveɪləns/

Definitions

  1. (n.) The regulatory process of monitoring the safety and effectiveness of a medical device or drug after it has been released on the market.
    The company implemented rigorous postmarket surveillance to identify any adverse effects of the new implant.

Forms

  • postmarket surveillance

Commentary

Often mandated by governmental agencies, postmarket surveillance aims to detect risks not identified during premarket approval, emphasizing continuous product safety monitoring.

This glossary is for general informational and educational purposes only. Definitions are jurisdiction-agnostic but reflect terminology and concepts primarily drawn from English and American legal traditions. Nothing herein constitutes legal advice or creates a lawyer-client relationship. Users should consult qualified counsel for advice on specific matters or jurisdictions.

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