Equipment and Resources. Subscriber is solely responsible for any travel, accommodations, computer equipment, telecommunications, and expenses required for Subscriber or its Users to access or use the Subscription.
Equipment and Resources a. [ * ] shall identify and purchase all reasonable Research and Development Equipment, except for the equipment identified in Section 6.b. below, to complete Phase I of this Agreement. Equipment described in this section will be housed at the Joint Laboratory in Honolulu, Hawaii.
Equipment and Resources. You must ensure that your Participants have access to adequate resources, materials and equipment (including but not limited to, a computer or mobile device with adequate access to the Internet) to allow them to attend and participate in the relevant Training Services. We can provide you on request with details of the required resources, materials and equipment for the relevant Training Services.
Equipment and Resources. This section of the evaluation is to verify if the Tenderer has available the required plant and equipment to successfully execute the works. The aim is to establish whether the Plant is owned or rented and if it is currently engaged in other works. The type, size and number of machinery and purpose in which the machine shall be evaluated. The tenderer must also include Plant and equipment plan reflecting the technical details and source of key plant and equipment offered. The bidder is required to attach documentary evidence of owned equipment or committed to lease from the supplier of the plant to be rented. The minimum equipment that will be ascertained for each tender is: No. Plant/Equipment List Minimum Number 1 Mobile cranes/ Crane Trucks (min 5 ton) 1 2 Dozers (min D6) 1
Equipment and Resources. Client is solely responsible for any travel, accommodations, computer equipment, telecommunications, and expenses required for Client or its Users to access or use the Subscription.
Equipment and Resources. 1.1 Maintains domiciliary patient equipment minimum stock levels by purchasing new equipment and monitoring returns.
Equipment and Resources. [DELETE WHOLE APPENDIX IF NOT APPLICABLE] Sponsor-Provided Equipment ☐ Please check this box if no Equipment will be provided by the Sponsor Sponsor will provide the CE- / UKCA- / UKNI-Marked equipment identified below (“Sponsor Equipment”) for use by the Participating Organisation in the conduct or reporting of the Non-Interventional Study:
Equipment and Resources. (a) Any equipment or resource that the Company provides to employees to assist them in performing their duties remains the property of the Company or such other person or entity as is the legal owner immediately prior to the item being provided. All such items must be returned when an employee’s employment is terminated or upon request. The cost of any tools or equipment not returned will be deducted from any moneys owing to the employee.
Equipment and Resources. If one Party gives the other Party use of its equipment or other resources in connection with this Contract, that Party must:
Equipment and Resources. Where no Equipment/Resources are being provided Appendix 7 should be omitted from the final clinical trial agreement. Appendix 7 includes tables where equipment and resources that are provided by Sponsors (and/or CROs, as applicable) for the clinical trial should be listed. These tables include a column where the depreciated value of the equipment/resources can be detailed. It is noted that there is no standard method for determining depreciation and therefore, this must be discussed and agreed between Sponsor and Participating Organisation (and CRO, as applicable). The Sponsor (or CRO, as applicable) should indicate whether alternative 1 or 2 should be used with respect to liability in Clause 7.2 of Appendix 7. The selection should be clearly indicated in the agreement. It is noted that Northern Ireland does not have any MIA arrangements and that the MIA in England is not applicable to equipment loaned or gifted for the purpose of clinical trials. Alternative #1 must be used where the Participating Organisation is constituted in England or Northern Ireland. Appendix 8 (CRO-mCTA only): Sponsor’s Clinical Trial Related Duties and Functions Under ICH-GCP to be Performed by CRO This Appendix should clearly set out which Sponsor responsibilities for site management will be performed by the CRO. If the Sponsor has formally empowered the CRO to sign this Agreement and thereby legally bind the Sponsor to its terms as a Party, this must be explicitly evidenced. Appendix 9 (Appendix 8 CRO mCTA): Formal Delegation of Authority from Sponsor to a Corporate Affiliate to Contractually Bind the Sponsor as a Party to this Agreement Where applicable, attach here evidence of formal delegation of authority, from the Sponsor to the corporate Affiliate of the Sponsor, to sign this Agreement and thereby legal bind the Sponsor to its terms as a Party. Contact Points for Advice and Assistance For queries relating to the use of the mCTAs for trials taking place in England: please contact the Health Research Authority, at xxxx@xxx.xxx.xx. For queries relating to use in Wales: please contact the Health and Care Research Wales Support and Delivery Centre at xxxxxxxx-xxxxxxxxx@xxxxx.xxx.xx. For queries relating to use in Scotland: please contact NHS Research Scotland at xxxxxxxxx@xxx.xxx.xx.
