Project Products Sample Clauses

Project Products. The CONSULTANT shall submit deliverables, detailed in Section IV of the RFP. The consultant shall also provide electronic and hard copy originals suitable for reproduction of all products to become the property of HCAOG.
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Project Products. The CONSULTANT shall submit deliverables, detailed in the Scope of Work. The consultant shall provide electronic files suitable for reproduction of all products to become the property of HCAOG.
Project Products. There will be two major products. The first, due 90 days from project start, will be an alternatives report that identifies the major issues and design choices available for the project. It will be similar in scope to the Interstate MAX Conceptual Design Report dated October 8, 1999, which was prepared by SOJ. The second major product will be a Final Conceptual Design Report that will be issued in September following additional technical work and a complete public review of alternatives. PROJECT COST Xxxxx Xxxxxxx 450 $140 63,000 Xxxx Xxxxxx 195 $170 33,150 Xxx Xxxx 250 $85 21,250 Xxxxx Xxxxxx 30 $180 5,400 Xxx Xxxxxx 100 $150 15,000 Total Fee $137,800 Reimbursables 10,000 *Based upon 120-day Scope of Work for Phase I of the Conceptual Design Phase EXHIBIT A Rev. 07/00 CONTRACTOR CERTIFICATION I, undersigned, am authorized to act on behalf of entity designated below, hereby certify that entity has current Workers' Compensation Insurance. Signature_________________________________ Date_________________________ Entity_______________________ ORS 670.600 Independent contractor; standards. As used in various provisions of ORS Chapters 316, 656, 657, and 701, an individual or business entity that performs labor or services for remuneration shall be considered to perform the labor or services as an "independent contractor" if the standards of this section are met. The contracted work meets the following standards:
Project Products. Each of the above outcomes will be generated by the project products: • Outcome 1 generated by two products: o A network of officials responsible for the management of protected aquatic ecosystems has been established, o the International Conference “Protecting the Biodiversity of the Adriatic”, which will bring together all project target groups. • Outcome 2 generated by three products: o The Boka Aquarium conservation center has been focused on public institutions responsible for the protection of biodiversity of the sea, local self-government units, academic institutions, non-governmental organizations and the general public; o Established freshwater aquarium “Skadar Lake”, focused on public institutions responsible for the protection of freshwater ecosystems, local government units, academic institutions, non-governmental organizations and the general public; o Established Wildlife Rescue Center, focused on public institutions responsible for the protection of biodiversity of the sea, local self-government units, academic institutions, non-governmental organizations and the general public. • Outcome 3 generated by five products: o Developed communication platform for stakeholder participation in the protection of water biodiversity, available for all target groups; o Developed WEB portal “Aquarium of Montenegro”, focused on all target groups; o Ensured gender equality, relevant to all target groups; o Established status of blue shark (Prionace glauca) in the Adriatic Sea (sea-water species), focused on public institutions responsible for the protection of biological diversity of the sea, academic institutions, non-governmental organizations and the general public; o Established status of European eel (Anguilla anguilla) in Skadar Lake (freshwater lead species) is focused on public institutions responsible for the protection of freshwater ecosystems, academic institutions, non-governmental organizations and the general public. • Outcome 4 generated by four products: o Workshop “EC Directive 92/43 / EEC (Habitats)”, o Workshop “EC Directive 1999/22 / EC (Zoo)”, o Workshop “EC Regulations No. 338/97 (CITES)”, “EC Regulation No. 865/2006 (CITES)”, “EU Regulation No. 791/2012 (CITES)”, o Workshop “EU regulation 1143/2014 (Invasive foreign species)”,
Project Products. NPS substantial involvement in the project should be evident in Article III. “
Project Products. Financial Reports: The recipient must submit Standard Form (SF) 425, “Federal Financial Report” (FFR), on a quarterly/semi-annual/annual basis. The FFRs may be submitted using one of the following methods: One original, mailed to: Contracting Division, National Park Service, Pacific West Regional Office, 000 Xxxx Xxxxxx, Suite 500, San Francisco, CA 94104 One scanned copy, emailed to: XXX_Xxxxxxxxxx@xxx.xxx Electronic submission through FedConnect The recipient will report program outlays and program income on a cash or accrual basis. The first interim FFR will be due in accordance with the following table: January 1 – March 31 June 30 July 30 April 1 – June 30 September 30 October 30 July 1 – September 30 December 31 January 30 October 1 – December 31 March 31 April 30 Subsequent interim FFRs are due 30 calendar days after the end of each federal fiscal quarter which ends on December 31, March 31, June 30, and September 30. The final FFR will be submitted 90 calendar days after the end of the term of agreement, or upon termination. Transactions which occurred after the award expired will also be included in the final reports. These expenses shall include wrap-up activities incurred during the project period and where the transaction occurred after the award expired. Transactions for the entire award period will be included in this final report and will reflect the transactions for the entire award amount. All financial and programmatic records submitted by recipients, supporting documents, statistical records, and other grants-related records shall be maintained in accordance with 2 CFR § 200.333. Performance Reports: The recipient must submit performance reports on a quarterly/semi-annual/annual basis. (Note: the Awarding Officer may waive performance reports if not needed, pursuant to 2 CFR 200.328(f), however, the justification for waiving the performance report requirement must be documented in the award file) The performance reports may be submitted using one of the following methods: One original, mailed to the ATR at the address shown in Article V, and to the following: Contracting Division, National Park Service, Pacific West Regional Office, 000 Xxxx Xxxxxx, Suite 500, San Francisco, CA 94104 One copy, emailed to the ATR at the email address shown in Article V, and to the following: XXX_Xxxxxxxxxx@xxx.xxx Electronic submission through FedConnect The performance reports must detail the following, in accordance with 2 CFR §200.328: A comparison of ...

Related to Project Products

  • 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.

  • 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.

  • Additional Products and Services Subject to the allocation of funds, the CPO may add similar equipment, supplies, services, or locations, within the scope of this Agreement, to the list of equipment, supplies, services, or locations to be performed or provided by giving written notification to Contractor. For purposes of this Section, the “Effective Date” means the date specified in the notification from the CPO. As of the Effective Date, each item added is subject to this Agreement, as if it had originally been a part, but the charge for each item starts to accrue only on the Effective Date. In the event the additional equipment, supplies, services, or locations are not identical to the items(s) already under this Agreement, the charges therefor will then be Contractor’s normal and customary charges or rates for the equipment, supplies, services, or locations classified in the Fees and Costs (Exhibit “F”).

  • Products Products available under this Contract are limited to Software, including Software as a Service, products and related products as specified in Appendix C, Pricing Index. Vendor may incorporate changes to their product offering; however, any changes must be within the scope of products awarded based on the posting described in Section 1.B above. Vendor may not add a manufacturer’s product line which was not included in the Vendor’s response to the solicitation described in Section 1.B above.

  • Additional Products Upon satisfying the minimum order requirements above, Enrolled Affiliate may order Additional Products.

  • Commercialization Intrexon shall have the right to develop and Commercialize the Reverted Products itself or with one or more Third Parties, and shall have the right, without obligation to Fibrocell, to take any such actions in connection with such activities as Intrexon (or its designee), at its discretion, deems appropriate.

  • 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.

  • Manufacture of Products All Products marketed through Grantor's Web ------------------------- Site shall be manufactured, packaged, prepared, and shipped in accordance with the specifications and requirements described on Exhibit A hereto as it may be modified from time to time. Quality control standards relating to the Product's weight, color, consistency, micro-biological content, labeling and packaging are also set forth on Exhibit A. In the event that Exhibit A is incomplete, Products shall be manufactured and shipped in accordance with industry standards.

  • 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.

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