Neuroscience Sample Clauses

Neuroscience. St. Mary’s College of Maryland (SMCM) welcomes students from College of Southern Maryland into our community of learners. This Articulation Agreement is designed to facilitate College of Southern Maryland students' ease of transfer from the Mathematics and Sciences: Biology Concentration program at College of Southern Maryland to the SMCM Neuroscience program. This Agreement augments any Guaranteed and Dual Admission agreements signed between The College of Southern Maryland and SMCM. Under this Agreement, College of Southern Maryland students graduating with an Associate of Science (A.S.) in Mathematics and Sciences: Biology Concentration will be eligible for admission into SMCM Neuroscience program, provided that students:
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Neuroscience. WP7: Non-invasive phenotyping of animal models for neurodegenarative diseases - WP8: with the following Sub-Workpackages - WP8.1: Identification of novel neuro-imaging targets in neurodegenarative diseases - WP8.2: Early diagnosis of neurodegenarative diseases - WP9: Neuroinflammation - WP10: Stem cell trafficking in the CNS TOPIC 2.2 Cardiovascular - WP11: with the following Sub-Workpackages - WP11.1: Multimodality characterization of atherosclerotic plaques - WP11.2: Characterization of myocardial angiogenesis - WP12: Cardiac stem cell therapy monitored by Molecular Imaging TOPIC 2.3 Inflammation & Regeneration - WP13: Molecular Imaging of NF-κB activation and imaging chronic inflammation using optical probes The composition of the Workpackages for research activities and their respective leaders are listed in Appendix 4. - Two (2) Workpackages for Dissemination and Spreading of Activities: - WP15.1: Activities of the Board of Training (BOT) - WP15.2: Activities of the Board of Dissemination and Communication (BODIC) Activities to spread excellence will be managed by the Board of Training (BOT), the Board of Dissemination and Communication (BODIC) and the Board for Knowledge and IPR Management (BOKIM), chaired by the Administrator for Knowledge Management (AKM). - One (1) Workpackage for Management Activities: - WP16: Management Activities Modification of Workpackage Any modification to the Workpackage’s representation shall be decided by the SMB which shall then appoint a new representation from amongst the Contractors involved in the relevant Workpackage, on the basis of proposition(s) made by the relevant Workpackage’ members by written way. Such a modification shall be considered as accepted by the Contractors involved in the relevant Workpackage if within fifteen (15) calendar days from receipt thereof, none of them has objected in writing to the Coordinator. Any objection to such a modification shall be submitted for determination to the Governing Board.
Neuroscience. Timing Major Milestones with respect to expected results, achievements, deliverables Start of Program • Establishment of in- and exclusion criteria for all patient groups • Specification of ethical aspects with particular emphasis on patients with degenerative brain disorders and dementia and national regulations • Specification of ethical aspects in animal models with particular emphasis on national regulations • Specification on animal mobility amongst the different partners to allow consecutive multimodal imaging Year 1 • Phenotyping of rat models for Xxxxxxxxx and Huntington Disease • Phenotyping of mice models for Amyotrophic Lateral Sclerosis • Establishment of [11C](R)-PK11195 in other DiMI laboratories • Implementation of protocols for MR-imaging • BBB, microglial probes or tPA probes validated • Establishment of the ability of tPA and tPAstop-tPA complexes to cross the blood-brain barrier and tissue distribution • Initial in-vivo studies in models of cerebral ischemia • Biochemical inflammatory markers, gene expression, and proteomics in patients • Annual implementation plan for Year 2 Year 2 • Phenotyping of primate models for Xxxxxxxxx and Huntington Disease • Implementation of animal brain atlases for automatic VOI definitions • Initial histopathological validation of current neuroimaging markers of inflammation • Initial blood-brain barrier integrity studies in patients with multiple sclerosis • Cross-sectional MR and/or PET in patients with MS, parkinsonism, memory dysfunction, HD, and prion disease • Paramagnetically labeled tPA made available to other partners • Biochemical inflammatory markers, gene expression, and proteomics in patients • Annual implementation plan for Year 3 Year 3 • Improved multimodality diagnostic tools for Alzheimer Disease mice models • Improved in vivo amyloid detection in Alzheimer Disease models • Implementation of new probes derived from Topic 1.2 in other DiMI-centres • Publication: MR-methodology of Q-space and BBB passage in MS patients • Publication: New tracers for microglia activation: Validation study • Publication: tPA probes validation study • Publication: in-vivo studies in models of cerebral ischemia • Establishment of the ability of tPA and tPAstop-tPA complexes to cross the blood-brain barrier and tissue distribution • Initial in-vivo studies in models of cerebral ischemia • Biochemical inflammatory markers, gene expression, and proteomics in patients • Annual implementation plan for Year 4 Year 4 •...
Neuroscience. (a) For each Neuroscience Phenomap, following completion of the applicable Stage 0 Plan, including selection of the Cell Context, the applicable JTT will finalize the Other Map Perturbations to be included in such Neuroscience Phenomap (and, if necessary, amend the applicable Research Plan to include such Other Map Perturbations) and, following agreement on the Phenomap Standards, Recursion will create a [***] Neuroscience Phenomap in such Cell Context, in accordance with such Research Plan; provided that, at Roche’s request, Recursion will not create a [***] Phenomap for such Cell Context (and the Stage 0-1 Activities solely applicable to such [***] Phenomap will be deemed discontinued) and instead will create a [***] Phenomap in such Cell Context as set forth in Section 3.3.2(b).
Neuroscience. (a) Promptly upon Recursion’s completion of each Neuroscience Phenomap, Recursion will provide Roche with written notice of such completion, which shall include data demonstrating achievement of the Phenomap Standards for such Phenomap. During the [***] day period following Roche’s receipt of such notice and data (the “Evaluation Period”), Recursion will permit and facilitate the full access (but not the ability to download) for up to [***] named individuals from, and nominated by, Roche to such Neuroscience Phenomap and the Neuro Image Data used to create such Phenomap, including the ability to query such Phenomap, solely to evaluate Roche’s interest in accepting such Phenomap. For clarity, any observations made pursuant to such queries shall be Collaboration Insights, to the extent they satisfy Section 1.32. For clarity, [***] in such Phenomap for purposes of Roche’s access during the applicable Evaluation Period and, to the extent Roche Small Molecules are included in such Phenomap, at least a subset of reference compounds comprising such Roche Small Molecules will be identified. Recursion will retain the right to maintain an Access Log of all queries to such Phenomap made during such Evaluation Period to monitor compliance with the Agreement. If, during the Evaluation Period for a Phenomap, Roche notifies the applicable JTT that it has concerns about the accuracy, functioning or reliability of such Phenomap, the applicable JTT shall promptly meet to discuss and determine how to address such concerns.

Related to Neuroscience

  • Manufacturing Technology Transfer With respect to each Technology Transfer Product, upon AbbVie’s written request after the Inclusion Date for the Included Target to which such Technology Transfer Product is Directed, Morphic shall effect a full transfer to AbbVie or its designee (which designee may be an Affiliate or a Third Party manufacturer) of all Morphic Know-How and Joint Know-How relating to the then-current process for the Manufacture of such Technology Transfer Product (the “Manufacturing Process”) and to implement the Manufacturing Process at facilities designated by AbbVie (such transfer and implementation, as more fully described in this Section 5.3, the “Manufacturing Technology Transfer”). To assist with the Manufacturing Technology Transfer, Morphic will make its personnel reasonably available to AbbVie during normal business hours for up to [***] FTE hours with respect to each Included Target (in each case, free of charge to AbbVie) to transfer and implement the Manufacturing Process under this Section 5.3. Thereafter, if requested by AbbVie, Morphic shall continue to perform such obligations; provided, that AbbVie will reimburse Morphic for its full-time equivalent (FTE) costs (for clarity, in excess of [***] FTE hours) and any reasonable and verifiable out-of-pocket costs incurred in providing such assistance. CERTAIN CONFIDENTIAL INFORMATION CONTAINED IN THIS DOCUMENT, MARKED BY [***], HAS BEEN OMITTED BECAUSE IT IS NOT MATERIAL AND WOULD LIKELY CAUSE COMPETITIVE HARM TO THE COMPANY IF PUBLICLY DISCLOSED.

  • Baxter and Nexell shall cooperate in any action taken by a third party solely involving a nullity action, opposition, reexamination or any other action taken by such third party alleging the invalidity or unenforceability of any Licensed Intellectual Property. Both parties agree to share equally in the cost of the defense of such Licensed Intellectual Property.

  • Technology Transfer Subject to the terms of the Development Supply Agreement, as soon as reasonably practicable, but in no event later than the fifth (5th) anniversary of the Effective Date, Alnylam shall initiate a technology transfer to MedCo, or to its Third Party manufacturer(s) of Licensed Product, selected by MedCo and reasonably acceptable to Alnylam, of Alnylam Know-How that is reasonably necessary or useful for the Manufacture of the Licensed Product, and shall make available its personnel on a reasonable basis to consult with MedCo or such Third Party manufacturer(s) with respect thereto, all at MedCo’s expense, including the Costs reasonably incurred by Alnylam in connection with such technology transfer activities. MedCo shall reimburse Alnylam such Costs incurred with respect to such Manufacturing technology transfer within [***] days after receipt of an invoice therefor. Alnylam and its Affiliates shall keep complete and accurate records in sufficient detail to enable the payments payable hereunder to be determined. Alnylam shall not be required to perform technology transfer to more than one Third Party manufacturer for each stage of the Licensed Product supply chain (i.e., Bulk Drug Substance, Bulk Drug Product and Finished Product). Promptly after MedCo’s written request, Alnylam shall use Commercially Reasonable Efforts to assign to MedCo any manufacturing agreement between Alnylam and a Third Party that is solely related to the manufacture of Licensed Products. Such assignment shall be subject to the terms and conditions of such agreement, including any required consents of such Third Party and MedCo’s written agreement to assume all the obligations of Alnylam under such agreement to be undertaken after such assignment, but Alnylam shall remain solely responsible for its obligations under such agreement arising prior to such assignment. Except as provided in the immediately preceding sentence, MedCo shall be solely responsible for contracting with such Third Party manufacturer (and any other Third Party manufacture to whom Alnylam has initiated technology transfer as set forth in this Section 5.3) for the supply of such Licensed Product and Alnylam shall have no obligations under such agreement between MedCo and such Third Party manufacturer. Alnylam shall use Commercially Reasonable Efforts to obtain any such consent in a form reasonably acceptable to MedCo.

  • 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.

  • Cornerstone shall notify the LLC and confirm such advice in writing (i) when the filing of any post-effective amendment to the Registration Statement or supplement to the Prospectus is required, when the same is filed and, in the case of the Registration Statement and any post-effective amendment, when the same becomes effective, (ii) of any request by the Securities and Exchange Commission for any amendment of or supplement to the Registration Statement or the Prospectus or for additional information and (iii) of the entry of any stop order suspending the effectiveness of the Registration Statement or the initiation or threatening of any proceedings for that purpose, and, if such stop order shall be entered, Cornerstone shall use its best efforts promptly to obtain the lifting thereof.

  • Technology Discoveries, innovations, Know-How and inventions, whether patentable or not, including computer software, recognized under U.S. law as intellectual creations to which rights of ownership accrue, including, but not limited to, patents, trade secrets, maskworks and copyrights developed under this Agreement.

  • Research Funding Genocea shall pay to Isconova in total [* * *] payable as follows: (i) $[* * *] in equal monthly installments for each remaining month in 2009 following the Effective Date and (ii) $[* * *] in equal monthly installments during the period from January 1, 2010 until March 31, 2012. The Research Funding shall be used solely for the performance of activities under the Research and Phase 1 Supply Plan and the Development and Scale-Up Plan and, for the avoidance of doubt, solely to fund Development and research activities for human (and not veterinary) applications in accordance with such Research and Phase 1 Supply Plan and Development and Scale-Up Plan. Notwithstanding anything to the contrary above, the Parties agree that this restriction shall only apply to the allocation and use of the Research Funding as such, and shall not be construed as limiting or affecting the ownership of any Isconova Technology and Joint Technology created, conceived, reduced to practice or Invented hereunder. Isconova’s ownership and/or rights to the Isconova Technology and Joint Technology shall exclusively be governed by the provisions in Section 3.3. and Isconova’s use of the Isconova Technology and Joint Technology shall be subject only to the licenses granted to Genocea in Sections 3.1.1 through 3.1.3. Isconova shall during the Research Term allocate not less than two (2) dedicated FTEs for Isconova’s research work for Genocea hereunder and each such dedicated FTE shall be paid through Research Funding. During the Research Term, Isconova shall, within fifteen (15) days after the end of each month, deliver to Genocea a report setting forth the number of Isconova FTEs that worked on activities under the Development and Scale-Up Plan and the Research and Phase 1 Supply Plan, as well as other costs and expenses of Isconova evidencing recourses spent on Isconova’s research work hereunder. Researching Funding THIS EXHIBIT HAS BEEN REDACTED AND IS THE SUBJECT OF A CONFIDENTIAL TREATMENT REQUEST. REDACTED MATERIAL IS MARKED WITH [* * *] AND HAS BEEN FILED SEPARATELY WITH THE SECURITIES AND EXCHANGE COMMISSION. payments shall be made within fifteen (15) days after the end of each calendar month.

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

  • Manufacturing and Marketing Rights The Company has not granted rights to manufacture, produce, assemble, license, market, or sell its products to any other person and is not bound by any agreement that affects the Company's exclusive right to develop, manufacture, assemble, distribute, market, or sell its products.

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