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Research License Agreement
"I need a Research License Agreement under Swiss law for a biotech startup licensing gene-editing technology from a Zurich-based university, with commercialization rights and a 5-year term starting January 2025."
1. Parties: Identification of the licensor and licensee, including full legal names and addresses
2. Background: Context of the research, relationship between parties, and purpose of the agreement
3. Definitions: Detailed definitions of key terms used throughout the agreement
4. License Grant: Scope of the license, permitted uses, and any territorial or field restrictions
5. Research Scope: Detailed description of permitted research activities and any limitations
6. Intellectual Property Rights: Ownership of background IP, foreground IP, and improvements
7. Confidentiality: Protection of confidential information, including research data and results
8. Payment Terms: License fees, research costs, and payment schedules if applicable
9. Representations and Warranties: Basic warranties regarding IP ownership and right to license
10. Liability and Indemnification: Limitation of liability and indemnification obligations
11. Term and Termination: Duration of agreement and termination conditions
12. General Provisions: Standard clauses including governing law, jurisdiction, and notices
1. Commercialization Rights: Include when there's potential for commercial exploitation of research results
2. Publication Rights: Include for academic research to address publication permissions and procedures
3. Data Protection: Include when research involves personal data processing
4. Export Control: Include for research involving controlled technologies or international transfers
5. Human Subjects Research: Include when research involves human subjects or clinical data
6. Material Transfer: Include when physical materials are being transferred for research
7. Quality Control: Include when specific research quality standards must be maintained
8. Reporting Requirements: Include when regular research progress reports are required
1. Schedule 1 - Licensed Technology: Detailed description of the licensed technology or research materials
2. Schedule 2 - Research Plan: Detailed research methodology, timelines, and deliverables
3. Schedule 3 - Fee Schedule: Detailed breakdown of all applicable fees and payment terms
4. Schedule 4 - Required Reports: Format and frequency of required research reports
5. Appendix A - Safety Protocols: Safety procedures and requirements for conducting research
6. Appendix B - Data Handling Procedures: Protocols for data collection, storage, and sharing
7. Appendix C - Quality Standards: Required quality control measures and standards
8. Appendix D - Contact Details: Key contacts for both parties for various aspects of the agreement
Authors
Life Sciences
Biotechnology
Pharmaceuticals
Information Technology
Medical Devices
Academic Research
Chemical Industry
Agricultural Science
Environmental Science
Materials Science
Artificial Intelligence
Robotics
Clean Technology
Healthcare
Legal
Research and Development
Intellectual Property
Compliance
Technology Transfer
Scientific Affairs
Business Development
Contracts Administration
Innovation
Academic Affairs
Regulatory Affairs
Research Director
Chief Scientific Officer
Legal Counsel
IP Manager
Technology Transfer Officer
Research Scientist
Laboratory Manager
Compliance Officer
Licensing Manager
Contract Administrator
Chief Technology Officer
Research Program Manager
Innovation Director
Academic Affairs Director
Partnership Manager
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