Examples of Research Institutions in a sentence
Subject to the terms of this Agreement, Gene-Cell hereby grants to Athersys the nonexclusive, limited license, including the right to sublicense to Research Institutions solely as permitted in Section 2.1, under the Gene-Cell Know-How and Gene-Cell Patents solely to conduct Athersys' obligations under the Research Program.
Each of the undersigned collaborating physicians ("Co-Investigators"), acting as either the Research Institution's employee or agent, will be primarily responsible, together with Principal Investigator, for performing the obligations of Principal Investigator in the Agreement.
Subject to the foregoing, Athersys may engage one or more research institutions as Athersys may deem necessary and appropriate ("Research Institutions"), subject to Gene-Cell's approval, which shall not be unreasonably withheld, to perform certain of Athersys' obligations under the Research Program; provided, however, that such Research Institution shall perform such work in compliance with the terms and conditions of this Agreement.
Notwithstanding anything to the contrary in this Article 3, neither Party shall be restricted from entering into any agreement with Controlled Contractors or Research Institutions with respect to any Sandoz MFN Projects.
The Company further understands and acknowledges that, pursuant to the Danish Act on Inventions at Public Research Institutions, the Hospital is entitled to, in its own discretion, either take over the intellectual property rights and title in and to such invention or to let such intellectual property rights and title remain with the inventors, in which case such intellectual property rights shall not be encompassed by this Framework Agreement.
Lead Investigator shall be responsible for notifying all of the Research Institutions and Principal Investigators of such termination.
Lead Institution, including Lead Investigator, shall maintain, and Lead Institution shall cause all Research Institutions and Principal Investigators to maintain, complete, accurate and current Clinical Study records for its Study Subjects as set forth in the Protocol ("Study Records").
Each of the undersigned collaborating physicians ("Co-Investigators"), acting as either the Research Institution's employee or agent, will be primarily responsible, together with investigator, for performing the obligations of Investigator in the Agreement.
In addition, Lead Institution agrees to, and will ensure that all Research Institutions, hold unblinded patient data for at least three (3) months after the completion of the Clinical Study.
If the IRB withdraws approval of the Clinical Study at any time, the Lead Investigator shall immediately notify Laboratory and the Research Institutions in writing and concurrently provide a written explanation of the circumstances leading to such withdrawal.