Common Contracts

Contract

December 11th, 2018

• Filed
  December 11th, 2018

The Parties agree as follows: Smluvní strany se dohodly takto: ARTICLE 1 CONDUCT OF THE STUDY ČLÁNEK 1PROVÁDĚNÍ KLINICKÉHO HODNOCENÍ 1.1 S tudy Standards. The Institution shall permit the Investigator to conduct the below mentioned 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"). 1.1 S tandardy Klinického hodnocení. Zdravotnické zařízení povolí zkoušejícímu provést níže uvedené Klinické hodnocení v souladu s (i) podm