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Research Service Agreement
"I need a Research Service Agreement for a pharmaceutical research project between our UAE-based laboratory and a German university, starting March 2025, focusing on clinical trial management with strict data protection requirements and publication rights provisions."
1. Parties: Identification of the contracting parties, including full legal names, addresses, and registration details
2. Background: Context of the agreement, including the purpose of the research and high-level objectives
3. Definitions: Definitions of key terms used throughout the agreement
4. Scope of Services: Detailed description of the research services to be provided
5. Term and Timelines: Duration of the agreement and key project milestones
6. Payment Terms: Financial terms, including fees, payment schedule, and expenses
7. Intellectual Property Rights: Ownership and licensing of research outputs, background IP, and foreground IP
8. Confidentiality: Protection of confidential information and research data
9. Data Protection and Privacy: Compliance with UAE data protection laws and data handling requirements
10. Representations and Warranties: Standard warranties regarding capability, authority, and quality of services
11. Liability and Indemnification: Allocation of risks and responsibilities between parties
12. Force Majeure: Provisions for unforeseen circumstances affecting performance
13. Termination: Conditions and procedures for ending the agreement
14. Governing Law and Jurisdiction: Specification of UAE law and dispute resolution procedures
1. Ethics and Compliance: Required when research involves human subjects or sensitive areas requiring ethical oversight
2. Publication Rights: Include when academic or public dissemination of research results is contemplated
3. Equipment and Facilities: Needed when specific research equipment or facilities are provided by either party
4. Personnel Requirements: Include when specific qualifications or security clearances are required for research staff
5. Export Control: Required when research involves controlled technologies or international collaboration
6. Insurance: Include when research activities carry significant risks requiring specific insurance coverage
7. Third-Party Rights: Needed when research involves third-party materials or collaborators
8. Regulatory Compliance: Include for research in regulated sectors (e.g., healthcare, pharmaceuticals)
1. Schedule 1 - Research Project Plan: Detailed description of research methodology, objectives, and deliverables
2. Schedule 2 - Fee Schedule: Detailed breakdown of fees, payment milestones, and eligible expenses
3. Schedule 3 - Key Personnel: List of key researchers and their qualifications
4. Schedule 4 - Technical Specifications: Specific technical requirements and standards for the research
5. Schedule 5 - Data Management Plan: Procedures for data collection, storage, and handling
6. Appendix A - Reporting Templates: Standard formats for progress reports and deliverables
7. Appendix B - Compliance Certificates: Copies of relevant regulatory approvals and certifications
8. Appendix C - Background IP Register: List of pre-existing intellectual property brought to the project
Authors
Background Intellectual Property
Business Day
Confidential Information
Data Protection Laws
Deliverables
Effective Date
Foreground Intellectual Property
Force Majeure Event
Good Industry Practice
Intellectual Property Rights
Key Personnel
Materials
Milestone
Project
Project Plan
Research Services
Research Data
Research Methodology
Research Objectives
Research Results
Service Fee
Service Level Requirements
Site
Specifications
Term
Third Party Materials
Work Product
UAE
Applicable Laws
Authorized Representative
Completion Date
Commencement Date
Contract Year
Data Subject
Ethics Approval
Funding
Good Research Practice
Implementation Plan
Information Security Requirements
License
Personal Data
Progress Report
Quality Standards
Records
Research Facility
Research Protocol
Schedule of Services
Statement of Work
Technical Information
Territory
Test Results
Timeline
Term and Duration
Research Services
Service Provider Obligations
Client Obligations
Payment Terms
Intellectual Property Rights
Confidentiality
Data Protection
Research Ethics
Quality Standards
Reporting Requirements
Key Personnel
Facilities and Equipment
Records and Audits
Warranties and Representations
Liability and Indemnification
Insurance
Force Majeure
Termination
Consequences of Termination
Assignment and Subcontracting
Compliance with Laws
Health and Safety
Publication Rights
Dispute Resolution
Governing Law and Jurisdiction
Notices
Entire Agreement
Variation
Severability
Third Party Rights
Export Control
Anti-Bribery and Corruption
Research Materials
Site Access
Change Control
Risk Management
Business Continuity
Information Security
Regulatory Compliance
Technology Transfer
Background Checks
Conflict of Interest
Healthcare and Life Sciences
Technology and Innovation
Education and Academia
Environmental Sciences
Energy and Sustainability
Manufacturing and Industrial
Financial Services
Aerospace and Defense
Agricultural Sciences
Biotechnology
Artificial Intelligence and Data Science
Materials Science
Pharmaceutical Research
Smart Cities and Infrastructure
Legal
Research and Development
Scientific Affairs
Compliance
Intellectual Property
Contract Management
Business Development
Innovation
Operations
Technical Services
Project Management
Quality Assurance
Regulatory Affairs
Finance
Procurement
Research Director
Legal Counsel
Chief Scientific Officer
Head of R&D
Research Project Manager
Intellectual Property Manager
Chief Technology Officer
Research Compliance Officer
Contract Manager
Principal Investigator
Business Development Manager
Innovation Director
Research Operations Manager
Technical Director
Scientific Affairs Manager
Research Administrator
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