MDRs definition
MDRs means medical device reports of adverse events required to be filed by medical device manufacturers and user facilities pursuant to Regulatory Laws of jurisdictions in which human clinical studies have been conducted (including observational studies) or other clinical use has occurred.
MDRs has the meaning ascribed to it in Section 7.1(f).
MDRs as defined in Section 3.11(d).
More Definitions of MDRs
MDRs has the meaning as defined in Section 1.4.
MDRs means Medical Device Reports, as defined and required by the FDA.
MDRs shall have the meaning set forth in Section 3.32 hereof.
MDRs has the meaning set forth in Section 4.9(d).