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Supply and Use Sample Clauses

Supply and Use. Idorsia owns or has the necessary rights to the Study Drug. Idorsia or its corporate affiliate will provide the Study Drug to Institution at no cost. Institu- tion and Investigator; (i) will verify to Idorsia receipt of the Study Drug; (ii) will store the Study Drug in a safe and se- curely-locked area as per Protocol require- ments; (iii) will use Study Drug only for Study purposes and according to the Pro- tocol; (iv) will limit access to the Study Drug only to those Study Personnel who are under Investigator's direct control; (v) will not dispense expired Study Drug to Subjects; and (vi) will not transfer the 1.7 Hodnocený přípravek.
Sample 1Sample 2See All (6)
Supply and Use. Idorsia owns or has the necessary rights to the Study Drug. Idorsia or its corporate affiliate will provide the Study Drug to Institution at no cost. Institution and Investigator; (i) will verify to Idorsia receipt of the Study Drug; (ii) will store the Study Drug in a safe and securely-locked area as per Protocol requirements; (iii) will use Study Drug only for Study purposes and according to the Protocol; (iv) will limit access to the Study Drug only to those Study Personnel who are under Investigator's direct control; (v) will not dispense expired Study Drug to Subjects; and (vi) will not transfer the Study Drug or any portion thereof to any third party without first obtaining written approval from Idorsia. 1.7.1 Xxxxxx a užívání. Společnost Idorsia vlastní Hodnocený přípravek nebo má k němu všechna nezbytná práva. Společnost Idorsia nebo její spřízněná společnost poskytne Zdravotnickému zařízení Hodnocený přípravek bezplatně. Zdravotnické zařízení a Zkoušející: (i) potvrdí společnosti Idorsia převzetí Hodnoceného přípravku; (ii) uchovávají Hodnocený přípravek na bezpečném a bezpečně uzamčeném místě v souladu s požadavky Protokolu; (iii) užívají Hodnocený přípravek výhradně pro účely provádění Klinického hodnocení a v souladu s Protokolem; (iv) omezí přístup k Hodnocenému přípravku pouze na ty Pracovníky podílející se na klinickém hodnocení, kteří jsou pod přímou kontrolou Zkoušejícího; (v) nevydávají Subjektům exspirované Hodnocený přípravek; a
Sample 1
Supply and Use. Idorsia owns or has the necessary rights to the Study Drug. Idorsia will provide the Study Drug, placebo to Institution at no cost. Institution and Investigator; (i) will verify to Idorsia receipt of the Study Drug; (ii) will store the Study 1.7
Sample 1
Supply and Use. The Provider shall supply the Material and the Provider Know-how to the Recipient at the premises of the Recipient. Risk in the Material [and the Provider Know-how] shall pass to the Recipient on delivery. The Recipient shall: only use the Material, Provider IPR and Provider Know-how for the Purpose during the Term in compliance with good laboratory practice, the highest standards of skill and care and all applicable laws and regulations [and the Provider's instructions concerning storage and use of the Materials]; ensure that the personnel handling the Material are apprised of any known hazards and warrants that they are qualified by training and experience to perform the Purpose; the Material is not for use in humans, in clinical trials, or for diagnostic purposes involving human subjects without the written consent of the Provider; the Recipient will not use any of the Materials for any commercial purpose or commercially-sponsored research without the prior written consent of the Provider which consent may be granted at the Provider’s sole discretion; and the Material is not to be given or made available to any third party or person, except Recipient’s employees, consultants, contract research organizations or collaborators that are bound by terms and conditions similar to the terms and conditions that are contained herein and shall not be used for any purpose other than for the Purpose. All requests for the Material from a third party other than Recipient’s employees, consultants, contract research organizations or collaborators will be referred to the Provider.
Sample 1
Supply and Use. Actelion owns or has the necessary rights to the Study Drug. Actelion or its corporate affiliate will provide the Study Drug to Institution at no cost. Institution and Investigator; (i) will verify to Actelion receipt of the Study Drug; (ii) will store the Study Drug in a safe and securely- locked area per Protocol requirements; (iii) will use Study Drug only for Study purposes and according to the Protocol; (iv) will limit access to the Study Drug only to those Study Personnel who are under Investigator's direct control; (v) will not dispense expired Study Drug to Subjects; and (vi) will not transfer the Study Drug or any portion thereof to any third party without first obtaining written approval from Actelion.
Sample 1
Supply and Use. Actelion owns or has the necessary rights to the Study Drug. Actelion or its corporate affiliate will provide the Study Drug to Institution at no cost. Institution and Investigator; (i) will verify to Actelion receipt of the Study Drug; (ii) will store the Study Drug in a safe and securely- locked area per Protocol requirements; (iii) will use Study Drug only for Study purposes
Sample 1
Supply and Use 
Sample 1

Related to Supply and Use

  • 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.

  • TRANSPORT SERVICES Upon the conclusion of such multilateral negotiations, the Parties shall conduct a review for the purpose of discussing appropriate amendments to this Agreement so as to incorporate the results of such multilateral negotiations.

  • Transportation Services i) In the event that transportation services for a student served by CONTRACTOR pursuant to an Individual Services Agreement are to be provided by a party other than CONTRACTOR or the LEA or its transportation providers, such services shall be reflected in a separate agreement signed by the parties hereto, and provided to the LEA and SELPA Director by the CONTRACTOR. Except as provided below, CONTRACTOR shall compensate the transportation provider directly for such services, and shall charge the LEA for such services at the actual and reasonable rates billed by the transportation provider, plus a ten percent (.

  • Transportation and Delivery Prices shall include all charges for packing, handling, freight, distribution, and inside delivery. Transportation of goods shall be FOB Destination to any point within thirty (30) days after the Customer places an Order. A Contractor, within five (5) days after receiving a purchase order, shall notify the Customer of any potential delivery delays. Evidence of inability or intentional delays shall be cause for Contract cancellation and Contractor suspension.

  • 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.

  • Transportation Transportation expenses include, but are not limited to, airplane, train, bus, taxi fares, rental cars, parking, mileage reimbursement, and tolls that are reasonably and necessarily incurred as a result of conducting State business. Each State agency shall determine the necessity for travel, and the mode of travel to be reimbursed.

  • Supply of Products ‌‌ 3.1 The Supplier warrants that the Products shall: (a) correspond with their description and any applicable Product Specification; (b) conform in all respects with the Order and any relevant sample; (c) be of satisfactory quality and fit for any purpose held out by the Supplier or made known to the Supplier by Ornua, expressly or by implication, and in this respect Ornua relies on the Supplier's skill and judgement; (d) be manufactured by properly trained and qualified personnel using all reasonable skill, care and diligence and in a good and workmanlike manner;‌ (e) where they are manufactured products, be free from defects in design, materials and workmanship and remain so for the period set out in the Product Specification or, if none is specified, for at least 12 months after delivery; (f) comply with all applicable statutory and regulatory requirements relating to the manufacture, labelling, packaging, storage, handling and delivery of the Products;‌ (g) comply with all relevant standards including any UK Standards, European Standards or International Standards applicable in the UK and the country or State where the Products are to be used; and (h) in the case of Products containing food stuffs, when delivered to Ornua, comply with all applicable food and hygiene legislation and regulations and best industry practice.‌ 3.2 The Supplier shall ensure that at all times it has and maintains all licences, permissions, authorisations, consents and permits needed to carry out its obligations under the Contract in respect of the supply of Products. Breach of this Condition shall be deemed a material breach of the Contract. 3.3 Ornua may inspect and test the Products at any time before delivery. The Supplier shall remain fully responsible for the Products despite any such inspection or testing and any such inspection or testing shall not reduce or otherwise affect the Supplier's obligations under the Contract. 3.4 If following such inspection or testing Ornua considers that the Products do not comply or are unlikely to comply with the Supplier's undertakings at clause 3.1, Ornua shall inform the Supplier and the Supplier shall immediately take such remedial action as is necessary to ensure compliance.‌ 3.5 Ornua may conduct further inspections and tests after the Supplier has carried out its remedial actions.

  • Specific Services Contractor shall provide the services described in Exhibit “A” attached hereto. No additional services shall be performed by Contractor unless approved in advance in writing by the County stating the dollar value of the services, the method of payment, and any adjustment in contract time or other contract terms. All such services are to be coordinated with County and the results of the work shall be monitored by the Director of Health and Human Services Agency or his or her designee.

  • SHIPPING AND AIR TRANSPORT 1. Profits of an enterprise of a Contracting State from the operation of ships or aircraft in international traffic shall be taxable only in that State. 2. The provisions of paragraph 1 shall also apply to profits from the participation in a pool, a joint business or an international operating agency.

  • Diagnostic Services Procedures ordered by a recognized Provider because of specific symptoms to diagnose a specific condition or disease. Some examples include, but are not limited to:

Most Referenced Clauses

Most Referenced Definitions