Joint Research and Development Sample Clauses

Joint Research and Development. Aspire and HEM may agree from time to time, in writing, to perform joint research and development activities on a project by project basis for products, procedures, processes and technology not forming part of the Technology or otherwise subject to this Agreement. The Intellectual Property, and other terms generated from such joint research and development activities, will be subject to a separate agreement, which will be negotiated separately among the Parties. Support for Clinical Trials. In relation to clinical trials of the Product undertaken by Aspire, Aspire shall be responsible for specifics costs, as outlined in Appendix D.
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Joint Research and Development. Accuray and AS&E may agree to engage in joint development of improvements or other technology related to the Products (“R&D”) and in particular with regard to (i) detection systems for use by domestic and foreign commercial, government and military customers for security related purposes, and (ii) detection and inspection systems for use in government and commercial non-destructive evaluation of finished products of component quality (collectively, “Security Systems”). The allocation of the costs of such R&D and the ownership of any rights, title and interest in and to the intellectual property resulting from such R&D shall be agreed between the parties in writing on a case-by-case basis prior to the commencement of any such R&D.
Joint Research and Development. 2.01 The parties hereto agree to combine their research and development efforts and to share the costs, risks and rights relating to the development of the ECRM Products, related and successor technology (whether or not foreseen at the time hereof), and such other items as the parties may agree to from time to time, including both basic or experimental research and product-specific research (whether relating to new product development or the improvement, adaptation or modification of existing products, as well as the development of prototypes) which the parties may agree to make part of the joint ECRM Products research and development program. The parties hereto intend that the arrangements contemplated by this Agreement constitute a "qualified cost contribution arrangement" pursuant to subsection 247(1) of the INCOME TAX ACT, Canada.
Joint Research and Development. GM and Quantum shall use their best ------------------------------ efforts to jointly develop Statements of Work for product research and development as further set forth in the Development Agreement.
Joint Research and Development 

Related to Joint Research and Development

  • Research and Development (i) Advice and assistance in relation to research and development of Party B;

  • Joint Development If joint development is involved, the Recipient agrees to follow the latest edition of FTA Circular 7050.1, “Federal Transit Administration Guidance on Joint Development.”

  • Clinical Development Licensee will have sole responsibility for and sole decision making over the clinical development of any Product arising from the Research Program in the Field. Notwithstanding the foregoing, if Licensee wishes to conduct clinical development of a Development Candidate at Penn and Penn has the clinical expertise, interest and ability to run such a trial as assessed at Penn’s sole discretion, such a study will be conducted under a separate Clinical Trial Agreement to be negotiated by the Parties prior to initiation of such study. Such separate clinical trial agreement will include a detailed clinical development plan, including costs and time lines for conducting the Clinical Trial.

  • Collaboration Management Promptly after the Effective Date, each Party will appoint a person who will oversee day-to-day contact between the Parties for all matters related to the management of the Collaboration Activities in between meetings of the JSC and will have such other responsibilities as the Parties may agree in writing after the Effective Date. One person will be designated by Merck (the “Merck Program Director”) and one person will be designated by Moderna (the “Moderna Program Director,”) together will be the “Program Directors”. Each Party may replace its Program Director at any time by notice in writing to the other Party. Any Program Director may designate a substitute to temporarily perform the functions of that Program Director by written notice to the other Party. The initial Program Directors will be: For Moderna: [***] For Merck: [***]

  • Development 3.3 Within twenty (20) Working Days after the Commencement Date and in accordance with paragraphs 3.10 to 3.12 (Amendment and Revision), the Contractor will prepare and deliver to the Authority for approval the full and final Security Plan which will be based on the draft Security Plan set out in Appendix B.

  • Business Development Provide advice and assistance in business growth and development of Party B. 业务发展。对乙方的业务发展提供建议和协助。

  • Business Development Company Buyer is a business development company as defined in Section 202(a)(22) of the Investment Advisors Act of 1940.

  • Research Support opioid abatement research that may include, but is not limited to, the following:

  • Initial Development Plan Not later than the Effective Date, Licensee shall have provided Merck with an initial Development plan for the Licensed Product in the Field in the Territory, which shall be incorporated as part of this Agreement as Attachment 3.02(a) (as may be amended in accordance with this Agreement, the “Development Plan”). **CERTAIN INFORMATION IN THIS EXHIBIT HAS BEEN OMITTED AND WILL BE FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION PURSUANT TO A CONFIDENTIAL TREATMENT REQUEST.

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