Common use of Independent Ethics Committee Clause in Contracts

Independent Ethics Committee. Provider and Principal Investigator will ensure that Trial is initiated only after both the Trial and the informed consent form (“ICF”) are approved by an IEC that complies with all Applicable Law. Provider and Principal Investigator will further ensure that the Trial is subject to continuing oversight by the IEC throughout its conduct. 4.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Independent Ethics Committee. Provider Institution and Principal Investigator will ensure that Trial is initiated only after both the Trial and the informed consent form (“ICF”) are approved by an IEC that complies with all Applicable LawLaw where Sponsor and/or its designee, INC Research, ensures the approval of the IEC. Provider and Principal Investigator Sponsor and/or its designee, INC Research, will further ensure that the Trial is subject to continuing oversight by the IEC throughout its conduct. 4.

Appears in 1 contract

Samples: Clinical Trial Agreement

Independent Ethics Committee. Provider and Principal Investigator will ensure that the Trial is initiated only after both the Trial and the informed consent form (“ICF”) are approved by an IEC that complies with all Applicable Law. Provider and Principal Investigator will further ensure that the Trial is subject to continuing oversight by the IEC throughout its conduct. 4.

Appears in 1 contract

Samples: Clinical Trial Agreement

Independent Ethics Committee. Provider and Principal Investigator INC Research will ensure that Trial is initiated only after both the Trial and the informed consent form (“ICF”) are approved by an IEC that complies with all Applicable Law. Provider Institution and Principal Investigator will further ensure that the Trial is subject to continuing oversight by the IEC throughout its conduct. 4.

Appears in 1 contract

Samples: Clinical Trial Agreement

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Independent Ethics Committee. Provider Institution and Principal Investigator will ensure that Trial is initiated only after both the Trial and the informed consent form (“ICF”) are approved by an IEC that complies with all Applicable Law. Provider Institution and Principal Investigator will further ensure that the Trial is subject to continuing oversight by the IEC throughout its conduct. 4.

Appears in 1 contract

Samples: Clinical Trial Agreement

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