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Research License
"I need a Research License Agreement for a Canadian biotechnology company to license its proprietary cell culture technology to a university research lab for a 2-year cancer research project starting March 2025, with strict confidentiality requirements and publication approval process."
1. Parties: Identification of the licensor and licensee, including full legal names and addresses
2. Background: Context of the research license, including the nature of research and general purpose
3. Definitions: Definitions of key terms used throughout the agreement
4. Grant of License: Scope and nature of the license being granted, including any field restrictions
5. Term and Termination: Duration of the license and conditions for termination
6. Research Parameters: Detailed description of permitted research activities and limitations
7. Intellectual Property Rights: Ownership and rights related to background IP and newly created IP
8. Confidentiality: Obligations regarding confidential information handling and protection
9. Publication Rights: Terms governing the publication of research results
10. Reporting Requirements: Requirements for progress reports and research documentation
11. Warranties and Indemnities: Standard warranties and indemnification provisions
12. General Provisions: Standard boilerplate clauses including governing law, notices, and assignment
1. Commercial Applications: Include when there's potential for commercial exploitation of research results
2. Data Protection: Required when research involves personal or sensitive data collection
3. Ethics and Compliance: Necessary for medical or human subject research
4. Export Control: Include when research involves controlled technologies or international collaboration
5. Government Funding: Required when research involves public funding or grants
6. Safety Protocols: Include for research involving hazardous materials or procedures
7. Student Involvement: Include when research involves students or academic institutions
8. Third-Party Rights: Required when research involves third-party materials or collaborators
1. Schedule A - Research Project Description: Detailed description of the research project, methodology, and objectives
2. Schedule B - Licensed Materials: Detailed list and description of materials covered by the license
3. Schedule C - Fee Schedule: Details of any fees, royalties, or financial arrangements
4. Schedule D - Reporting Template: Standard format for required research progress reports
5. Schedule E - Security Requirements: Specific security protocols for handling research materials
6. Appendix 1 - Background IP: Detailed list of pre-existing IP brought to the research
7. Appendix 2 - Approved Research Team: List of authorized researchers and their qualifications
8. Appendix 3 - Research Facilities: Description of approved facilities where research can be conducted
Authors
Life Sciences
Information Technology
Biotechnology
Pharmaceuticals
Environmental Sciences
Engineering
Healthcare
Agriculture
Clean Technology
Materials Science
Artificial Intelligence
Medical Devices
Aerospace
Chemical Industry
Energy
Legal
Research & Development
Intellectual Property
Regulatory Affairs
Technology Transfer
Compliance
Scientific Affairs
Innovation
Corporate Development
Academic Affairs
Licensing
Business Development
Research Director
Chief Scientific Officer
Legal Counsel
IP Manager
Technology Transfer Officer
Research Administrator
Principal Investigator
Head of R&D
Licensing Manager
Compliance Officer
Research Project Manager
Chief Technology Officer
Innovation Director
Scientific Program Manager
Research Coordinator
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