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Research Service Agreement
"I need a Research Service Agreement for a six-month clinical trial study starting March 2025, where my pharmaceutical company will engage a local Indonesian research institution to conduct human trials for a new diabetes medication, with strict confidentiality and data protection requirements."
1. Parties: Identification of the research service provider and the client, including their legal status and addresses
2. Background: Context of the research service arrangement and the parties' intentions
3. Definitions: Key terms used throughout the agreement
4. Scope of Services: Detailed description of the research services to be provided
5. Term and Timeline: Duration of the agreement and key milestone dates
6. Payment Terms: Financial arrangements, including fees, payment schedule, and expenses
7. Intellectual Property Rights: Ownership and usage rights of research outputs and pre-existing IP
8. Confidentiality: Protection of confidential information and research data
9. Research Standards and Compliance: Required research methodologies, ethics, and compliance with Indonesian regulations
10. Reporting and Deliverables: Required research outputs, reports, and delivery specifications
11. Representations and Warranties: Parties' assurances regarding capacity and service quality
12. Limitation of Liability: Extent and limitations of parties' liabilities
13. Termination: Conditions and procedures for ending the agreement
14. General Provisions: Standard legal clauses including notices, amendments, and governing law
1. Data Protection: Required when research involves personal or sensitive data collection and processing
2. Export Control: Needed when research involves international data or material transfer
3. Publication Rights: Including when research results may be published in academic contexts
4. Third-Party Rights: Required when external collaborators or subcontractors are involved
5. Equipment and Facilities: Needed when specific research equipment or facilities are provided by either party
6. Insurance Requirements: Include when research involves high-risk activities or valuable equipment
7. Force Majeure: Optional but recommended for long-term research projects
8. Research Staff and Personnel: Required when specific personnel are key to the research delivery
1. Schedule 1 - Research Proposal: Detailed description of research methodology, objectives, and expected outcomes
2. Schedule 2 - Fee Schedule: Detailed breakdown of fees, payment milestones, and reimbursable expenses
3. Schedule 3 - Timeline and Deliverables: Detailed project timeline, milestones, and specific deliverables
4. Schedule 4 - Key Personnel: List of key researchers and their qualifications
5. Schedule 5 - Research Protocols: Specific research methodologies and procedures to be followed
6. Schedule 6 - Compliance Requirements: Specific regulatory and ethical requirements applicable to the research
7. Schedule 7 - Equipment and Materials: List of equipment and materials to be used or provided
8. Appendix A - Required Forms and Templates: Standard forms for reporting, consent, and other documentation
Authors
Life Sciences
Technology
Healthcare
Manufacturing
Agriculture
Environmental Sciences
Education
Pharmaceuticals
Energy
Mining
Telecommunications
Consumer Goods
Financial Services
Biotechnology
Chemical Industry
Legal
Research & Development
Compliance
Intellectual Property
Scientific Affairs
Contract Administration
Business Development
Innovation
Corporate Affairs
Risk Management
Research Director
Legal Counsel
Chief Scientific Officer
Research Project Manager
Contract Manager
Head of R&D
Compliance Officer
Intellectual Property Manager
Chief Technology Officer
Research Coordinator
Business Development Manager
Scientific Director
Research Administrator
Corporate Counsel
Innovation Manager
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