Selected article for: "adverse event and study adverse event"

Author: Bird, Grace; Braithwaite, Irene; Harper, James; McKinstry, Steven; Koorevaar, Iris; Fingleton, James; Semprini, Alex; Dilcher, Meik; Jennings, Lance; Weatherall, Mark; Beasley, Richard
Title: Protocol for a randomised, single-blind, two-arm, parallel-group controlled trial of the efficacy of rhinothermy delivered by nasal high flow therapy in the treatment of the common cold
  • Document date: 2019_6_19
  • ID: x2xc1s14_217
    Snippet: As sponsor, Fisher and Paykel Healthcare Ltd. will monitor the study according to their own procedures and will review all serious adverse events. All adverse events and device deficiencies will be reported to the study sponsor in accordance with current local and national adverse event reporting policies. The sponsor will manage device deficiency reports as part of its ongoing postmarketing safety review process......
    Document: As sponsor, Fisher and Paykel Healthcare Ltd. will monitor the study according to their own procedures and will review all serious adverse events. All adverse events and device deficiencies will be reported to the study sponsor in accordance with current local and national adverse event reporting policies. The sponsor will manage device deficiency reports as part of its ongoing postmarketing safety review process.

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