Common use of Study Standards Clause in Contracts

Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable written instructions (iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws, ordinances, rules, and regulations of any governmental authority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law").

Appears in 2 contracts

Samples: Clinical Trial Agreement, Clinical Trial Agreement

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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) IdorsiaActelion's reasonable written instructions (iv) generally accepted standards of good clinical practice; (v) the International Council on Harmonization of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws, ordinances, rules, and regulations of any governmental authority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law").

Appears in 1 contract

Samples: Clinical Study Agreement

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Study Standards. Institution and Investigator shall perform the Study in accordance with (i) the terms and conditions of this Agreement; (ii) the Protocol; (iii) Idorsia's reasonable written instructions (iv) generally accepted standards of good clinical clin- ical practice; (v) the International Council on Harmonization Harmonisation of Technical Requirements of Pharmaceuticals for Human Use Guideline for Good Clinical Practice (“ICH-GCP”); and (vi) all national and international laws, ordinances, rules, and regulations of any governmental authority au- thority ("Regulatory Authority") and any other authority that apply to the conduct of the Study or the activities contemplated hereunder ("Applicable Law"). zmocněným k poskytování určitých služeb v souvislosti s Klinickým hodnocením.

Appears in 1 contract

Samples: Institution Agreement

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