Study Devices Sample Clauses

The "Study Devices" clause defines the terms and conditions under which devices used in a clinical study are provided, managed, and handled by the parties involved. It typically outlines responsibilities for supplying, maintaining, and returning the devices, as well as requirements for their use, storage, and reporting of any malfunctions or adverse events. This clause ensures that all parties understand their obligations regarding the study devices, thereby promoting proper device management and compliance with regulatory standards throughout the study.
Study Devices. Records of receipt, use, or disposition of the study device, including receipt dates, serial and lot numbers, names of all persons who received or used the device, why and how many devices were returned to the study Sponsor or otherwise disposed of.
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Study Devices. Records of study device shipments and disposition shall be maintained. Records of shipments shall include the name and address of the consignee, type and quantity of devices shipped. Records of disposition shall describe the batch numbers of any devices returned to the Sponsor, repaired, or disposed of in other ways by the Investigator or another person, and the reasons for and method of disposal.
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Study Devices. Palomar agrees to support the Study by delivering the Study Devices, placing such Study Devices in proper operating condition for the conduct of the Study, and maintaining such Study Devices in such operating condition during the term of this Agreement, all at no charge to General. General and Principal Investigator shall have no liability for any failure to fulfill their obligations as a result of unavailability of a Study Device. Study Devices will remain Palomar's property unless otherwise agreed. The General and Principal Investigator shall safeguard such property with the degree of care used for its own property and, in accordance with Palomar's instructions at any time, shall return or otherwise dispose of all such property. General and Principal Investigator shall not use any Study Device for any purpose other than the Study, unless otherwise agreed.
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Study Devices. Sponsor shall provide all Study Devices (Investigational Devices) necessary for conduct of the Study to Institution and Principal Investigator at no charge, pursuant to the terms set forth below and the Agreement. Institution and Investigators shall not seek or retain payment from any subject, third-party payor or any other person or entity for the Investigational Device.
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Related to Study Devices

  • Fabrication Making up data or results and recording or reporting them.

  • Intercept Devices 26.1.1.1 Local and federal law enforcement agencies periodically request information or assistance from local telephone service providers. When either Party receives a request associated with an End User of the other Party, it shall refer such request to the Party that serves such End User, unless the request directs the receiving Party to attach a pen register, trap-and-trace or form of intercept on the Party's facilities, in which case that Party shall comply with any valid request.

  • Development Work The Support Standards do not include development work either (i) on software not licensed from CentralSquare or (ii) development work for enhancements or features that are outside the documented functionality of the Solutions, except such work as may be specifically purchased and outlined in Exhibit 1. CentralSquare retains all Intellectual Property Rights in development work performed and Customer may request consulting and development work from CentralSquare as a separate billable service.

  • Manufacture 2.1. The LED(s) on the LED module shall be equipped with suitable fixation elements. 2.2. The fixation elements shall be strong and firmly secured to the LED(s) and the LED module.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time. (b) The Supplier shall not change any process, material, component, packaging or manufacturing location without the Purchaser’s express prior written approval.