LIABILITIES AND RESPONSIBILITIES OF THE PARTIES Sample Clauses

LIABILITIES AND RESPONSIBILITIES OF THE PARTIES. In addition to the other liabilities and responsibilities described in this agreement the Investigator/Investigational Site is obliged to:
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LIABILITIES AND RESPONSIBILITIES OF THE PARTIES. In addition to the other liabilities and responsibilities described in this agreement the institution is obliged to: - act as the employer of the investigators, trial nurses and other personnel conducting the trial; - ensure that during the term of trial set forth in this agreement, the Investigators engaging in the trial do not initiate any other clinical trial at the trial site, which would delay recruitment of subjects for this trial; - ensure that qualified and instructed personnel and adequate equipment are available for the trial and that the trial may also in other respects be conducted in safe conditions; - allow participation of the Investigators and when appropriate/needed also trial nurses in Investigator meetings and other education arranged by the Sponsor; - ensure that the Investigators are familiar with the details of the protocol and other liabilities and responsibilities defined in this agreement, and that Investigators are committed to act accordingly; - ensure that the subjects are not simultaneously involved in any other clinical trials and that they are not subjects to any investigations differing from the trial protocol and - allow monitoring and auditing at the trial site to be conducted by the sponsor, as well as domestic and foreign regulatory authorities, and, if necessary, to assist in the executing thereof. In addition to the liabilities and responsibilities described in this agreement the sponsor of the trial is obliged to: - provide the institution with the necessary background information needed for the appropriate and safe conduct of the trial; - ensure necessary training and orientation of the investigators and other personnel of the institution involved in the trial in order to conduct the trial in accordance with the protocol. The training, meetings, and travelling related to the conduct of the trial shall be separately agreed between the sponsor of the trial, the institution, and investigators; - ensure that the trial is covered by a pharmaceutical injuries insurance policy, from which possible damages caused by the investigational medicine are compensated to the trial subjects in accordance with insurance conditions [attach when appropriate an insurance certificate]; - register the trial into an open international publication register according to common practice before starting the patient recruitment, as well as - inform the institution of the completion of the trial.

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