Product Formulations Sample Clauses

Product Formulations. The finished Product formulas and Specifications are owned exclusively by and shall have no rights of ownership in, or use of (except for such limited use as is required to perform its obligations under this Agreement), the Product formulas or Specifications. This includes, without limitation, license rights, excepting the license rights granted herein. Subject to the requirements of Section 3 and Section 23, nothing herein shall prohibit from developing product formulas and specifications within the normal course of conducting its business.
Sample 1
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Product Formulations. The Company has disclosed to Purchaser the percentages by weight of petroleum distillates, volatile organic compounds, Hazardous Materials and certain other (but not all) components for each current formula for the Company's chemical products, together with the Material Data Safety Sheets and product labels for such chemical products. To the Shareholders' knowledge, (i) the product labels for such products comply with Consumer Product Safety Commission guidelines, and (ii) the product formulations are accurately reflected in the disclosures in the Material Safety Data Sheets for these products.
Sample 1
Product Formulations. Senetek shall have the right (but not the obligation) to analyze Enprani's formulations of the Products for compliance with Senetek's efficacy and safety standards, which are as follows: Senetek shall provide its assay method to Enprani to conduct testing of any and all formulations produced and marketed by Enprani to insure that such formulations have less than [***] systemic absorption with a time interval of [***], such testing to utilize either mass spectrometry techniques or radioactive tracers. Senetek is granted with the right of analysis of random samples prior to Enprani's full production of the Product. Senetek reserves the right to update or change testing procedures and shall promptly give Enprani a written notice thereof. Senetek shall be afforded a period of fifteen (15) days upon receipt of the data to provide its written approval or disapproval of such formulations with written reasons for its decision. If no written response is received from Senetek within fifteen(15) days upon receipt of the data, such formulation shall be deemed approved. No approval of any formulation by Senetek shall be deemed an endorsement of such formulation or a determination by Senetek that such product is safe or effective, nor shall the same be implied by Enprani to any person or entity. After the manufacture of the Product has commenced, Enprani shall report to Senetek, from time to time, the analysis results for L random samples of the Units manufactured with lots specified. Senetek shall have the right to audit, at Senetek's expense, random samples of the product formulations once a year during normal business hours, and more frequently if an audit reveals that product formulation standards deviate from those standards stated herein.
Sample 1
Product Formulations. Sepracor shall be solely responsible for the formulation, indications, labeling and packaging for the Product. Sepracor may change any formulation, labeling, and/or packaging at its own discretion with thirty (30) days prior written notice to Xxxxxx, unless such change requires pre-approval by the FDA, in which case Sepracor shall obtain Xxxxxx'x prior written approval which shall be promptly given and not unreasonably withheld. Sepracor shall be responsible for the cost of such changes and the cost to change any and all Sepracor Promotional Materials.
Sample 1
Product Formulations. All formulations developed by Licensee relating to the Products shall be jointly owned by the parties. Upon completion of each such formulation approved by KOOP, Licensee shall deliver to KOOP all necessary and relevant information and documentation, in a mutually acceptable format, relating to each such formulation. The parties agree in good faith to work together to perform all necessary tasks relating to the protection of each party's ownership in the Product formulations.
Sample 1

Related to Product Formulations

  • 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.

  • 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 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.

  • 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.

  • Licensed Product “Licensed Product” shall mean any article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights. For clarity, a “Licensed Product” shall not include other product or material that (a) is used in combination with Licensed Product, and (b) does not constitute an article, composition, apparatus, substance, chemical material, method, process or service whose manufacture, use, or sale is covered or claimed by a Valid Claim within the Patent Rights.

  • 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.

  • API If the Software offers integration capabilities via an API, your use of the API may be subject to additional costs or Sage specific policies and terms and conditions (which shall prevail in relation to your use of the API). You may not access or use the API in any way that could cause damage to us or the Software, or in contravention of any applicable laws. We reserve the right in our sole discretion, to: (i) update any API from time to time; (ii) place limitations around your use of any API; and (iii) deny you access to any API in the event of misuse by you or to otherwise protect our legitimate interests.

  • 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.

  • 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.

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