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1. Parties: Identification of the license issuer (typically a government entity or authorized institution) and the license recipient (researcher or research organization)
2. Background: Context of the research license application and general purpose
3. Definitions: Key terms used throughout the license agreement, including technical and legal terminology
4. Scope of License: Detailed description of permitted research activities, fields of study, and geographical limitations
5. Duration and Renewal: Term of the license, renewal conditions, and procedures
6. Compliance Requirements: Mandatory regulatory requirements, reporting obligations, and compliance with UAE research laws
7. Research Standards: Required standards, methodologies, and ethical guidelines to be followed
8. Data Protection and Privacy: Requirements for handling research data, personal information, and confidential materials
9. Intellectual Property Rights: Ownership and usage rights of research outcomes, discoveries, and innovations
10. Reporting Requirements: Regular reporting obligations, progress updates, and documentation requirements
11. Termination: Conditions for license termination, suspension, or revocation
12. Governing Law: Confirmation of UAE law application and jurisdiction
1. International Collaboration: Required when research involves international partners or cross-border activities
2. Commercial Applications: Needed when research has potential commercial applications or industry partnerships
3. Environmental Impact: Required for research activities that may affect the environment
4. Human Subjects Research: Necessary when research involves human participants or clinical trials
5. Technology Transfer: Required when research involves import/export of technology or technical knowledge
6. Funding Arrangements: Needed when research involves external funding or financial sponsorship
7. Laboratory Requirements: Required for research involving laboratory facilities or specialized equipment
8. Insurance and Liability: Necessary when research activities carry significant risks or liability concerns
1. Schedule 1 - Research Project Description: Detailed outline of the research project, methodology, and objectives
2. Schedule 2 - Key Personnel: List of authorized researchers and their qualifications
3. Schedule 3 - Facility Details: Information about research facilities and locations
4. Schedule 4 - Compliance Checklist: Detailed regulatory compliance requirements and checkpoints
5. Schedule 5 - Safety Protocols: Safety procedures and emergency response plans
6. Appendix A - Required Forms: Standard forms for reporting and documentation
7. Appendix B - Fee Schedule: Applicable fees, charges, and payment terms
8. Appendix C - Equipment Register: List of authorized research equipment and tools
Healthcare and Medical Research
Biotechnology
Information Technology
Environmental Sciences
Energy and Sustainability
Artificial Intelligence and Robotics
Pharmaceutical Research
Agricultural Sciences
Materials Science
Space and Aviation
Chemical Research
Educational Research
Industrial Research and Development
Clean Technology
Defense and Security Research
Legal
Research and Development
Regulatory Affairs
Compliance
Operations
Scientific Affairs
Innovation
Laboratory Operations
Quality Assurance
Ethics Committee
Grant Administration
Research Administration
Intellectual Property
Technology Transfer
Clinical Research
Research Director
Chief Scientific Officer
Principal Investigator
Research Compliance Officer
Legal Counsel
Regulatory Affairs Manager
Research Project Manager
Laboratory Manager
Ethics Committee Chair
Research Administrator
Scientific Research Coordinator
Innovation Manager
Research Grant Manager
Clinical Research Director
Research Operations Manager
Chief Technology Officer
Head of R&D
Research Quality Assurance Manager
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