STUDY EQUIPMENT Sample Clauses

STUDY EQUIPMENT. [TO BE INSERTED IF APPLICABLE] Under this Agreement the SPONSOR will supply the INSTITUTION, for use in the Study, on............................(delivery date) following device […] (include description of the device, brand, type, serial number) (“EQUIPMENT”) on a loan-for-use or free lease base for the entire duration of the Study; The INSTITUTION shall examine the Equipment upon its delivery and shall verify if satisfactory to the INSTITUTION’s needs. The Equipment is a medical device for which the SPONSOR expressly confirms that the device complies with the terms and conditions laid down under applicable law. The current value of the device is………..EUR (exclusive of VAT). This is without prejudice to Institution’s liability with respect to the Equipment being limited to duly evidenced wilful misconduct and/or gross negligence of Institution.
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STUDY EQUIPMENT. On behalf of Sponsor, Pharm-Olam will provide at no cost to Institution and/or the Investigator refrigerator (“Equipment”). Upon the delivery of Equipment, Institution and/or Investigator will promptly inspect the Equipment and provide a written notice of acceptance to Pharm-Olam or Sponsor. The Institution and the Investigator shall ensure that the Equipment is maintained and controlled in accordance with the Pharm-Olam’s and Sponsor´s instructions, ICH/GCP guidelines, applicable laws and regulations, and in the manner outlined in the Protocol. The Institution and the Investigator acknowledge and agree that the Equipment shall be used for the sole purpose of conducting the Study in strict accordance with the Protocol and for no other purpose, and it shall not be transferred to any third parties. Any handling of the Equipment shall be reserved for Institution´s employees, Sub-Investigators, subcontractors, agents, affiliates, and related personnel who are under the Investigator’s direct control and who shall use the Equipment only as set forth herein. The Institution and the Investigator shall ensure that the Equipment is stored securely to prevent use by unauthorized persons and will otherwise observe reasonable safety measures customarily employed by the Institution and the Investigator with respect to similar equipment in their possession. In the event that the Equipment is lost, damaged, or destroyed while at the Institution or with the Investigator, the Institution and the Investigator shall be jointly and severally liable to Pharm-Olam and/or Sponsor for the Equipment, such liability shall cover,
Sample 1
STUDY EQUIPMENT. On behalf of Sponsor, Pharm-Olam will provide at no cost to Institution and/or the Investigator refrigerator (“Equipment”) terms of conditions shall be governed by separated loan agreement by and between Institution/Investigator and Pharm-Olam/Sponsor. Handover takes place based on the Handover form.
Sample 1
STUDY EQUIPMENT. On behalf of Sponsor, Pharm-Olam will provide at no cost to Institution refrigerator (“Equipment”) terms of conditions relating to the Equipment shall be governed by separated loan agreement by and between Institution and Pharm- Olam.
Sample 1
STUDY EQUIPMENT. To ensure that the XXXX R&D Office is notified if any medical equipment is to be donated or loaned to the Trust for the purposes of this study (i.e. ECG machine) prior to the first patient being recruited in the trial so that appropriate indemnity arrangements can be put in place.  To ensure that appropriate and up-to-date testing and calibration records are maintained for all equipment used for the purposes of this trial and that these records are made available for regulatory inspection or upon request by the Sponsor. Monthly reports  If a portfolio adopted study, to complete all reporting obligations required by the NEYNL CRN (accrual figures) and funding body. Annual reports  To send an Ethics annual progress report (APR) to the REC and XXXX R&D. The APR is due each year from the date of the ethics favourable opinion for the trial for the duration of the trial.  To send an MHRA annual Development Safety Update Report (DSUR) summarizing SAEs, SARs and SUSARs to the MHRA, REC and XXXX R&D. The DSUR is due each year from the date of MHRA clinical trial authorization for the duration of the trial. R&D will provide the template and guide to writing the DSUR. End of trial  Notify the MHRA, REC and XXXX R&D within 90 days of the trial completing using the Declaration of End of Trial form.  Notify the MHRA, REC and XXXX R&D if the study is terminated early (before the planned date of completion) within 15 days of the decision to end the study using the Declaration of End of Trial form.  Notify XXXX R&D immediately of any reason to halt the trial. Decide with XXXX R&D whether the trial should be halted temporarily. Notify the MHRA, REC and XXXX R&D within 15 days of a decision to temporarily halt the study by submitting a substantial amendment notification.  Note that if a trial has a REC favourable opinion and/or MHRA clinical trial authorisation but does not start and the decision is made not to continue with the study, then the REC and MHRA still require notifying on the Declaration of End of Trial form otherwise the REC and MHRA will require annual reports.  To resolve all actions following the study monitor’s closedown visit.  To send a copy of the summary of the clinical trial publication or final report to the MHRA, REC and Trust R&D within one year of the end of the trial including an analysis of all AEs, SAEs, SARs and SUSARs.  Initiate and coordinate review and submission of abstracts, posters and publications.  The content and timing of...
Sample 1
STUDY EQUIPMENT. On behalf of Sponsor, Pharm-Olam will provide at no cost to Institution and/or the Investigator refrigerator, machine read urine dipstick (in case of needs), min- max thermometers (“Equipment”). Upon the delivery of Equipment, Institution and/or Investigator will promptly inspect the Equipment and provide a written notice of acceptance to Pharm-Olam or Sponsor. The Institution and the Investigator shall ensure that the Equipment is maintained and controlled in accordance with the Pharm-Olam’s and Sponsor´s instructions, ICH/GCP guidelines, applicable laws and regulations, and in the manner outlined in the Protocol. The Institution and the Investigator acknowledge and agree that the Equipment shall be used for the sole purpose of conducting the Study in strict accordance with the Protocol and for no other purpose, and it shall not be transferred to any third parties. Any handling of the Equipment shall be reserved for Institution´s employees, Sub-Investigators, subcontractors, agents, affiliates, and related personnel who are under the Investigator’s direct control and who shall use the Equipment only as set forth herein. The Institution and the Investigator shall ensure that the Equipment is stored securely to prevent use by unauthorized persons and will otherwise observe reasonable safety measures customarily employed by the Institution and the Investigator with respect to similar equipment in their possession.
Sample 1

Related to STUDY EQUIPMENT

  • Safety Equipment Should the employment duties of an employee in the bargaining unit require use of any equipment or gear to insure the safety of the employee or others, the District agrees to furnish such equipment or gear.

  • Equipment Use Lessee agrees that the Equipment will be operated by competent, qualified personnel in connection with Lessee's business for the purpose for which the Equipment was designed and in accordance with applicable operating instructions, laws, and government regulations, and that Lessee shall use all reasonable precautions to prevent loss or damage to the Equipment from fire and other hazards. Lessee shall procure and maintain in effect all orders, licenses, certificates, permits, approvals, and consents required by federal, state, or local laws or by any governmental body, agency, or authority in connection with the delivery, installation, use, and operation of the Equipment.

  • Rental Equipment 7.1 We will at all times own all Rental Equipment supplied to you. You will not let, sell, charge, assign, sub-license or allow a third party to use the Rental Equipment nor remove any labels, and shall not prejudice our rights in the Rental Equipment in any way. We may replace the Rental Equipment from time to time either with your prior consent or provided that the replacement Rental Equipment is of a specification that is at least equal to the Rental Equipment originally supplied and such change does not materially disrupt the provision of the Services.

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