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.
Appears in 3 contracts
Samples: Investigator Agreement, Investigator Agreement, clinicaltrials.gov
Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies 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.
Appears in 3 contracts
Samples: Investigator Agreement, Investigator Agreement, Investigator Agreement
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 per the manufacturer’s guidelines.
Appears in 1 contract
Samples: Investigator Agreement
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.
Appears in 1 contract
Samples: Investigator Agreement
Device Deficiencies. Safety Assessment Assess and record any Device Deficiencies device deficiencies that are reported or observed observed, since the previous visit. Requirements for reporting device deficiencies in the study can be found in Section 11.
Appears in 1 contract
Samples: Investigator Agreement