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Research Service Agreement
"I need a Research Service Agreement for a pharmaceutical research project between our Nigerian biotech company and Lagos University, starting March 2025, with specific provisions for handling human tissue samples and data protection compliance."
1. Parties: Identification of the contracting parties with full legal names and addresses
2. Background: Context of the agreement and brief description of the research project
3. Definitions: Definitions of key terms used throughout the agreement
4. Scope of Services: Detailed description of the research services to be provided
5. Project Timeline and Deliverables: Specific timelines, milestones, and deliverables for the research
6. Payment Terms: Financial terms, payment schedule, and expense provisions
7. Intellectual Property Rights: Ownership and licensing of research results and pre-existing IP
8. Confidentiality: Protection of confidential information and research data
9. Regulatory Compliance: Compliance with relevant laws, regulations, and ethical requirements
10. Personnel and Resources: Key personnel commitments and resource allocation
11. Reports and Documentation: Requirements for research documentation and reporting
12. Term and Termination: Duration of agreement and termination provisions
13. Liability and Indemnification: Risk allocation between parties
14. Force Majeure: Provisions for unforeseen circumstances
15. General Provisions: Standard boilerplate clauses including governing law, notices, and amendment procedures
1. Human Subjects Research: Required when research involves human participants, including ethical compliance and informed consent procedures
2. Equipment and Materials: Include when specific research equipment or materials are provided by either party
3. International Collaboration: Required for cross-border research activities, including export control compliance
4. Publication Rights: Include when academic publication of research results is contemplated
5. Data Protection: Detailed section required when processing personal data or sensitive research data
6. Background IP License: Include when background intellectual property is being licensed for the research
7. Commercialization Rights: Required when there's potential for commercial exploitation of research results
8. Student Involvement: Include when students will be involved in the research activities
1. Schedule 1 - Research Protocol: Detailed description of research methodology and procedures
2. Schedule 2 - Budget and Payment Schedule: Detailed breakdown of costs and payment milestones
3. Schedule 3 - Key Personnel: List of key researchers and their qualifications
4. Schedule 4 - Timeline and Deliverables: Detailed project timeline with specific deliverables and deadlines
5. Schedule 5 - Equipment and Materials: List of equipment and materials to be used in the research
6. Schedule 6 - Reporting Templates: Standard formats for progress reports and final documentation
7. Appendix A - Compliance Requirements: Specific regulatory and ethical requirements applicable to the research
8. Appendix B - Background IP: List of relevant background intellectual property brought to the project
Authors
Healthcare and Life Sciences
Technology and Innovation
Education
Agriculture
Environmental Sciences
Energy
Manufacturing
Pharmaceuticals
Biotechnology
Social Sciences
Engineering
Mining and Natural Resources
Information Technology
Telecommunications
Legal
Research and Development
Compliance
Scientific Affairs
Contract Administration
Intellectual Property
Ethics
Data Protection
Project Management
Academic Affairs
Laboratory Operations
Quality Assurance
Regulatory Affairs
Research Director
Chief Scientific Officer
Legal Counsel
Research Project Manager
Principal Investigator
Contract Manager
Compliance Officer
Research Coordinator
Chief Technology Officer
Head of R&D
Research Scientist
Academic Dean
Laboratory Manager
Intellectual Property Manager
Data Protection Officer
Ethics Committee Chair
Research Administrator
Grant Manager
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