Common use of Device Deficiencies Clause in Contracts

Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies that are reported or observed since the previous visit. Requirements for reporting device deficiencies in the study can be found in Section 11. Device deficiencies on comparator lenses should be reported by the Investigator per the manufacturer’s guidelines.

Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies that are reported or observed since the previous visit. Requirements for reporting device deficiencies in the study can be found in Section 11. Device deficiencies on comparator lenses should be reported by the Investigator per the manufacturermanufacture’s guidelines. Note: Device deficiencies must be recorded for all enrolled subjects from the time of signature of informed consent, regardless of subject enrollment status (screen failure or randomized).

Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies device deficiencies that are reported or observed observed, including those associated with changes in concomitant medication dosing since the previous visit. Requirements for reporting device deficiencies in the study can be found in Section 11. Device deficiencies on comparator lenses should be reported by the Investigator per the manufacturer’s guidelines.

Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies that are reported or observed since the previous visit. Requirements for reporting device deficiencies in the study can be found in Section 11. Device deficiencies on comparator lenses should be reported by the Investigator per the manufacturer’s guidelines.