Ethics Committee (IEC. IRB) - An independent body (a review board or a committee, institutional, regional, national, or supranational), constituted of medical professionals and non-medical members, whose responsibility it is to ensure the protection of the rights, safety and well-being of Trial Subjects involved in the Study and to provide public assurance of that protection, by, among other things, reviewing and approving / providing favourable opinion on, the Protocol, the suitability of the Investigator(s), facilities, and the methods and material to be used in obtaining and documenting Informed Consent of the Trial Subjects.
Appears in 3 contracts
Samples: Clinical Trial Agreement, Clinical Trial Agreement, Clinical Trial Agreement
Ethics Committee (IEC. IRB) - An independent body (a review board or a committee, institutional, regional, national, or supranational), constituted of medical professionals and non-medical members, whose responsibility it is to ensure the protection of the rights, safety and well-being of Trial Subjects involved in the Study and to provide public assurance of that protection, by, among other things, reviewing and approving / providing favourable favorable opinion on, the Protocol, the suitability of the Investigator(s), facilities, and the methods and material to be used in obtaining and documenting Informed Consent of the Trial Subjects.
Appears in 1 contract
Samples: Clinical Trial Agreement