Initial Prototypes definition

Initial Prototypes means the six (6) Prototypes that Palomar is required pursuant to the R&D Plan to deliver to Gillette at or near the beginning of the R&D Period.
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Initial Prototypes means the * single-use Prototype Devices developed for delivery of the Initial Compound, * of which will serve as sample injectors. * This material has been omitted pursuant to a request for confidential treatment and has been filed separately with the Commission.
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Initial Prototypes means the six (6) Prototypes that Palomar is required pursuant to the R&D Plan to deliver to Xxxxxxxx at or near the beginning of the R&D Period. “Joint Excluded Inventions” shall mean any and all Information and Inventions that are first conceived, developed or reduced to practice jointly (as determined under U.S. patent law) by or on behalf of representatives, employees, agents or research partners of Palomar and representatives, employees, agents or research partners of Xxxxxxxx during the term of the Agreement, either together or jointly (as determined under U.S. patent law) with a Third Party(ies), on or after the Amendment Date and during the term of this Agreement to the extent constituting or comprising any (i) Topical, or (ii) Selected Topical Container. “Joint Excluded Know-How” shall mean all Information and Inventions included in the Joint Excluded Inventions that are not generally known, plus all Specific Property Rights arising from Joint Excluded Inventions, but excluding any Information and Inventions to the extent claimed by a Joint Excluded Patent. “Joint Excluded Patents” shall mean any Patents to the extent one or more claims of such Patents claim any Joint Excluded Inventions, provided that “Joint Excluded Patents” shall not include claims of such Patents to the extent that any such Joint Excluded Invention (a) is claimed in combination with any Light-Based Device and (b) enables the Functionality of such device. “Joint Excluded Technology” shall mean the Joint Excluded Patents and the Joint Excluded Know-How, collectively. “Joint Inventions” shall mean any and all Information and Inventions that are (a) first conceived, developed or reduced to practice jointly (as determined under U.S. patent law) by or on behalf of representatives, employees, agents or research partners of Palomar and representatives, employees, agents or research partners of Xxxxxxxx during the term of the Agreement, either together or jointly (as determined under U.S. patent law) with a Third Party(ies), (b) first conceived, developed or reduced to practice by or on behalf of representatives, employees, agents or research partners of Xxxxxxxx, either alone or jointly (as determined under U.S. patent law) with Third Party(ies) during the term of the Agreement in connection with activities arising from, or performed pursuant to, the R&D Plan, or in the course of performing Additional Activities or Commercial Assessment Period Additional Activities, or (c) first conce...
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Examples of Initial Prototypes in a sentence

  • Frecker, M., et al., Laparoscopic Multifunctional Instruments: Design and Testing of Initial Prototypes.

  • As promptly as is reasonably possible after agreement of the parties on the Initial Prototypes, Zarlink shall deliver to Given five hundred (500) prototypes of the Circuits in final production, chip scale packaging (the “Final Prototypes” and, together with the Initial Prototypes, the “Prototypes”), after testing the Prototypes to its satisfaction for basic compliance with the Circuit Specifications.

  • From 1 July 1993 to 30 March 1994, there were 636 conferences, out of which 326 fully settled and 84 partly settled.

  • Overall scores from all quantitative feedback are listed, along with a summary of 13 feedback and discussion that led to the listed conclusion about implementation.1 Table 5: Initial Prototypes, participant scoring and feedback, and conclusions 2PrototypeBrief Description clinical services, and support for pregnant people and young families one’s own neighborhood.

  • Phase 2 (running from month 10 to 24) – Baseline Data Collection, Initial Prototypes, First Evaluation and Requirements Refinement: Patient enrolment will take place and data acquisition will be started (Step 4).

  • DEVELOPMENT OF THE DEMONSTRATORS Testing Initial Prototypes The main objective of the original test campaigns was to investigate if standard cushions (i.e. “off the shelf” components) could be efficiently used for cylindrical objects/surfaces with a limited diameter.

  • SGA adopted a Groundwater Management Plan (GMP) for the management of the northern Sacramento County groundwater basin on Decem- ber 11, 2003.

  • Given shall have the right to request such adjustments and revisions to the Initial Prototypes as it deems appropriate and the parties shall negotiate in good faith any such adjustments and revisions.

  • Introduction 2 Executive Summary 3 Literature Review 5 Hypotheses 8 Surveys 10 Personas 15 Development 17 Initial Prototypes 18 User Testing 21 Final Prototype 28 Conclusion 32 1 Resources 33 INTRODUCTION Millennials are expected to travel more than any generation prior1, there should be an app that helps them and other groups of people plan trips together.


More Definitions of Initial Prototypes

Initial Prototypes and “Final Prototypes” are defined in Section 2.5.
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Initial Prototypes means the six (6) Prototypes that Palomar is required pursuant to the R&D Plan to deliver to Xxxxxxxx at or near the beginning of the R&D Period. “Joint Inventions” shall mean any and all Information and Inventions that are (a) first conceived or reduced to practice jointly (as determined under U.S. patent law) by or on behalf of representatives, employees, agents or research partners of Palomar and representatives, employees, agents or research partners of Xxxxxxxx during the term of the Agreement, either together or jointly (as determined under U.S. patent law) with a Third Party(ies), (b) first conceived or reduced to practice by or on behalf of representatives, employees, agents or research partners of Xxxxxxxx, either alone or jointly (as determined under U.S. patent law) with Third Party(ies) during the term of the Agreement in connection with activities arising from, or performed pursuant to, the R&D Plan, or in the course of performing Additional Activities or Commercial Assessment Period Additional Activities, or (c) first conceived or reduced to practice by or on behalf of representatives, employees, agents or research partners of Palomar, -vii-
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Related to Initial Prototypes

  • Electrical protection barrier means the part providing protection against any direct contact to the high voltage live parts.

  • Biological safety cabinet means a containment unit suitable for the preparation of low to moderate risk agents where there is a need for protection of the product, personnel, and environment, according to National Sanitation Foundation (NSF) Standard 49.

  • Development regulations or "regulation" means the controls

  • FFDCA means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. §301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Web Site Accessibility Standards/Specifications means standards contained in Title 1 Texas Administrative Code Chapter 206.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • ERCOT Protocols means the document adopted by ERCOT, including any attachments or exhibits referenced in that document, as amended from time to time, that contains the scheduling, operating, planning, reliability, and settlement (including customer registration) policies, rules, guidelines, procedures, standards, and criteria of ERCOT. For the purposes of determining responsibilities and rights at a given time, the ERCOT Protocols, as amended in accordance with the change procedure(s) described in the ERCOT Protocols, in effect at the time of the performance or non-performance of an action, shall govern with respect to that action.

  • Specifications means the Specifications of the Works included in the Contract and any modification or addition made or approved by the Project Manager.

  • Government Apprenticeship Programme “ means training which is funded by the Government via the National Apprenticeship Service.

  • Underground source of drinking water means an aquifer or its portion:

  • Prescription drug order means an original or new order from a practitioner for drugs, drug-related devices or treatment for a human or animal, including orders issued through collaborative care agreements. Lawful prescriptions result from a valid practitioner-patient relationship, are intended to address a legitimate medical need, and fall within the prescribing practitioner's scope of professional practice;

  • Flea and tick insecticide means any insecticide product that is designed for use against fleas, ticks, their larvae, or their eggs. “Flea and Tick Insecticide” does not include products that are designed to be used exclusively on humans or animals and their bedding.

  • Electronic and Information Resources Accessibility Standards means the accessibility standards for electronic and information resources contained in 1 Texas Administrative Code Chapter 213.

  • Commencement of Commercial Production means the first occurrence of Commercial Production in an Area.

  • Diagnostic clinical procedures manual means a collection of written procedures that describes each method (and other instructions and precautions) by which the licensee performs diagnostic clinical procedures; where each diagnostic clinical procedure has been approved by the authorized user and includes the radiopharmaceutical, dosage, and route of administration.

  • Analytical x-ray system means a group of components utilizing x-rays to determine the elemental composition or to examine the microstructure of materials.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Applicable water quality standards means all water quality standards to which a discharge is subject under the federal Clean Water Act and which has been (a) approved or permitted to remain in effect by the Administrator following submission to the Administrator pursuant to Section 303(a) of the Act, or (b) promulgated by the Director pursuant to Section 303(b) or 303(c) of the Act, and standards promulgated under (APCEC) Regulation No. 2, as amended.

  • Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.

  • Technical Specifications means the detailed requirements for the Work furnished by the Architect and set forth in Book 3 of the Contract Documents.

  • Procurement Regulations means, for purposes of paragraph 87 of the Appendix to the General Conditions, the “World Bank Procurement Regulations for IPF Borrowers”, dated July 2016, revised November 2017 and August 2018.

  • National Ambient Air Quality Standards or “NAAQS” means national ambient air quality standards that are promulgated pursuant to Section 109 of the Act, 42 U.S.C. § 7409.

  • District Specifications means the specifications followed by the State Government in the area where the work is to be executed.

  • Crawling bug insecticide means any insecticide product that is designed for use against ants, cockroaches, or other household crawling arthropods, including, but not limited to, mites, silverfish or spiders. “Crawling Bug Insecticide” does not include products designed to be used exclusively on humans or animals, or any house dust mite product. For the purposes of this definition only: