Medical Device Trial

/ˈmɛdɪkəl dɪˈvaɪs traɪəl/

Definitions

  1. (n.) A legally regulated clinical investigation conducted to evaluate the safety and effectiveness of a medical device before market approval or clearance.
    The medical device trial demonstrated the product's compliance with regulatory standards.

Forms

  • medical device trial
  • medical device trials

Commentary

Note that medical device trials differ from pharmaceutical trials due to device-specific regulatory requirements and often distinct endpoints.

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.

Draft confidently with Amicus

Create, negotiate, and sign agreements in one secure workspace—invite collaborators, track revisions, and keep audit-ready records automatically.

Open the Amicus app