Access to Product Sample Clauses

Access to Product. Subscriber acknowledges that the Product is a hosted software-as-a-service offering and that Subscriber is responsible for all hardware, software, connectivity and related infrastructure required for Subscriber and Users to access and use the Product. Without limiting the disclaimers and limitations of liability set out in the Blue J Legal Terms of Use, Blue J Legal disclaims any and all liability resulting from any impairment or disruption of the Subscriber’s access to the Product caused by the actions or inactions of third parties such as, but not limited to, Internet service providers.
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Access to Product. 3.1 ASXO will make the Product available to the Subscriber as soon as reasonably practicable following the commencement of this Agreement. 3.2 ASXO may amend this Agreement at any time, including discontinuing any Products, by giving 90 days’ prior written notice, but reserves the right to make urgent changes with less notice where reasonably necessary having regard to the nature of the event. The Subscriber may immediately terminate this Agreement without liability if the change is likely to be detrimental to the Subscriber. The Subscriber shall be entitled to a pro-rata refund for Fees paid in advance from the date of termination. 3.3 To request a variation to the Product the Subscriber will complete and sign a new Order Form. ASXO will treat such a request by the Subscriber as an offer and may accept that offer subject to the payment of ASXO’s then current Fees for the Product. 3.4 If ASXO accepts the Subscriber’s offer under clause 3.3, ASXO will issue an invoice and the parties agree to be bound by those amendments on and from the date of invoice.
Sample 1
Access to Product. 1.1. Subject to Section 1.5 and Dealer’s payment of fees and compliance with all other/the terms and conditions of this Agreement, Provider allows the Dealer to have access to and to use the Product via a web based user-interface and mobile application for the Licensed Use. 1.2. In order to allow Provider to grant Dealer access to the Product, Dealer will disclose to Provider the email address used to sign up for an account on “xxxxxxxxxxxxx.xx”. Provider will assign the necessary rights to Dealer’s account. 1.3. Provider grants Dealer access to the Product via the corresponding software over the internet. The installer file for the software running in the Dealer’s customer’s practice will be provided to Provider via download link. Since the availability and performance of the internet or the Dealer’s or the Dealer’s customer’s software does not form part of Provider’s responsibility, Provider shall not be liable to Dealer for any failure of the Product due to internet restrictions or the limitations of the functionality of such software at any time. 1.4. Dealer undertakes as follows: 1.4.1. Dealer shall be responsible to ensure that Dealer’s customer’s’ systems and the local networks where the Equipment is installed meet the conditions of application of the Product and system requirements as set by Provider and listed in the Product manual, during installation or connection of the Product and throughout the term of this Agreement. 0.0.0. Xxxxxx will immediately after installation ensure that the Product is assigned by the Dealer’s customer to Dealer as a “Service Partner” of such Dealer’s customer in the software, in order to establish the Licensed Use accordingly. 0.0.0. Xxxxxx is responsible to ensure that all access data to the Product or the IoT-platform from which the Product operates in accordance with this Section 1. All data derived or obtained from the Licensed Use is kept confidential by Dealer and secured from access of any third party in accordance with all healthcare and other laws, rules and regulations applicability to the security, confidentiality and privacy of data obtained and maintained by Dealer’s customer. 0.0.0. Xxxxxx will at any time immediately inform Provider about any change of address, or any relevant issue concerning the business of Dealer which can impact the execution of the service.
Sample 1
Access to Product. 8.4.1. Within [timing] the Partner shall deliver to FUNDER a Marketing Plan which will describe the Partner’s planned activities to make the Product available for stockpile in accordance with the definition of “Market” or otherwise in preparation for an Outbreak or Increased Outbreak Preparation Need. 8.4.2. Partner shall ensure that the first [w%] of doses of Product Manufactured in the first [v] years after scale-up shall be provided as directed in writing by FUNDER in accordance with the FUNDER Equitable Access Policy.
Sample 1
Access to Product. Customer must permit free and safe access to Covered Products and provide without charge to Entrust adequate storage space, working space and all necessary utilities for use by Entrust personnel.
Sample 1
Access to Product. Customer shall permit free and safe access to the Covered Product and shall provide without charge to Datacard such storage space, working space and necessary utilities as may be required by Datacard personnel to perform Standard Service.
Sample 1
Access to Product. Product is provided by means of granting to User access to the web-based portal at xxxxx.xxxxxxxxx.xxx ("Portal"). User will identify the username and password that are used for access to User's account on Portal. User will not share its username or password with any third party and will be responsible and liable for the acts or omissions of any person who accesses Product using passwords or access procedures provided to User. Kaspersky Lab reserves the right to refuse registration of, or to suspend or cancel, login IDs used by User to access the Product for any reason, including if User violates the terms and conditions set forth in this Agreement.
Sample 1
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Related to Access to Product

  • Commercialization License Subject to the terms of this Agreement, including without limitation Section 2.2 and Theravance's Co-Promotion rights in Section 5.3.2, Theravance hereby grants to GSK, and GSK accepts, an exclusive license under the Theravance Patents and Theravance Know-How to make, have made, use, sell, offer for sale and import Alliance Products in the Territory.

  • Third Party Products and Services Any third-party hardware, software and/or services that is delivered by ResMed for use either standalone or in conjunction with ResMed products and/or services, shall be subject to the third-party terms and conditions and/or license agreements between Customer and the third party. Such third-party hardware, software and/or services is provided by ResMed "AS IS," without any warranty of any kind. Any representations or warranties as to such hardware, software and/or services shall only be as granted by the applicable third parties, if any, that accompany such products and/or software and/or services. Any representations, warranties, or other similar obligations with respect to such third-party hardware, software and/or services flow directly from the third party to Customer and ResMed shall have no responsibility at all for any such representations, warranties, obligations or lack thereof.

  • PRODUCT MANUFACTURER'S SUPPLIERS Only those dealers/distributors listed by the manufacturer will be considered authorized to act on behalf of the Product Manufacturer.

  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

  • SHOP DRAWINGS, PRODUCT DATA AND SAMPLES 4.12.1 Shop Drawings are drawings, diagrams, schedules and other, data specially prepared for the Work by the Contractor or any Subcontractor, manufacturer, supplier or distributor to illustrate some portion of the Work. 4.12.2 Product Data are illustrations, standard schedules, performance charts, instructions, brochures, diagrams and other information furnished by the Contractor to illustrate a material, product or system for some portion of the Work. 4.12.3 Samples are physical examples which illustrate materials, equipment or workmanship and establish standards by which the Work will be judged. 4.12.4 The Contractor shall review, approve and submit, with reasonable promptness and in such sequence as to cause no delay in the Work or in the work of the State or any separate contractor, all Shop Drawings, Product Data and Samples required by the Contract Documents. 4.12.5 By approving and submitting Shop Drawings, Product Data and Samples, the Contractor represents that he / she has determined and verified all materials, field measurements, and field construction criteria related thereto, or will do so, and that he / she has checked and coordinated the information contained within such submittals with the requirements of the Work and of the Contract Documents. 4.12.6 The Contractor shall not be relieved of responsibility for any deviation from the requirements of the Contract Documents by the Architect's approval of Shop Drawings, Product Data or Samples under Subparagraph 2.2.7 of these General Conditions unless the Contractor has specifically informed the Architect and the State in writing of such deviation at the time of sub- mission and the Architect and the State has given written approval to the specific deviation. The Contractor shall not be relieved from responsibility for errors or omissions in the Shop Drawings, Product Data or Samples by the Architect's approval thereof. 4.12.7 The Contractor shall direct specific attention, in writing or on resubmitted Shop Drawings, Product Data or Samples, to revisions other than those requested by the Architect on previous submittals. 4.12.8 No portion of the Work requiring submission of a Shop Drawing, Product Data or Sample shall be commenced until the submittal has been approved by the Architect as provided in Subparagraph 2.2.7 of these General Conditions. All such portions of the Work shall be in accordance with approved submittals.

  • SINGLE-USE PRODUCTS The Board of County Commissioners has established a single-use products and plastic bags policy intended to reduce the use of products which have become globally recognized as having lasting negative impacts on the environment. Neither single-use products nor plastic bags may be sold or disbursed on County property by staff or contracted vendors, except as set forth in Orange County Administrative Regulation 9.01.03. Failure to comply with the Regulation may result in termination of the contract or other contractual remedies, and may affect future contracting with the County. The use of reusable, recyclable, biodegradable, or compostable materials is encouraged.

  • Product Labeling The labeling of all Licensed Products sold or offered for sale under this Agreement shall expressly state that the Licensed Product is manufactured under a license from the Medicines Patent Pool.

  • Licensed Product The term “Licensed Product” shall mean any product (a) the manufacture, use, importation, sale or offer for sale of which would, in the absence of the license granted by this Agreement, infringe a Valid Claim of any of the Licensed Patent Rights, or (b) that is comprised of, utilizes or incorporates Licensed Biological Materials, or (c) that is discovered, developed or made using a Licensed Process.

  • Licensed Products Lessee will obtain no title to Licensed Products which will at all times remain the property of the owner of the Licensed Products. A license from the owner may be required and it is Lessee's responsibility to obtain any required license before the use of the Licensed Products. Lessee agrees to treat the Licensed Products as confidential information of the owner, to observe all copyright restrictions, and not to reproduce or sell the Licensed Products.

  • New Products You agree to comply with NASD Notice to Members 5-26 recommending best practices for reviewing new products.

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