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Clinical Research Agreement
"I need a Clinical Research Agreement under German law for a Phase II oncology trial between BioPharma GmbH (sponsor) and University Hospital Munich (institution), with a planned start date of March 2025, including provisions for biological sample storage and multi-center trial coordination."
1. Parties: Identification of the contracting parties including the sponsor, institution, and principal investigator
2. Background: Context of the clinical trial, purpose of the agreement, and basic information about the study
3. Definitions: Definitions of key terms used throughout the agreement
4. Scope of Trial: Detailed description of the clinical trial, including objectives, protocol compliance requirements, and timeline
5. Responsibilities of Institution: Obligations of the research institution, including compliance with protocol, regulations, and reporting requirements
6. Responsibilities of Sponsor: Sponsor's obligations including provision of study drug, monitoring, and regulatory compliance
7. Principal Investigator Obligations: Specific duties and commitments of the principal investigator
8. Budget and Payment Terms: Financial terms, payment schedule, and cost coverage
9. Confidentiality: Confidentiality obligations and protection of proprietary information
10. Data Protection: GDPR compliance, data handling, and protection measures
11. Intellectual Property: Ownership and rights to study results, inventions, and publications
12. Publication Rights: Terms governing the publication of study results
13. Subject Injury and Indemnification: Liability allocation and compensation for trial-related injuries
14. Insurance: Insurance requirements and coverage specifications
15. Term and Termination: Duration of agreement and termination provisions
16. Governing Law and Jurisdiction: Specification of German law application and jurisdiction
17. General Provisions: Standard contractual provisions including notices, amendments, and assignment
1. Multi-Center Trial Provisions: Additional terms for multi-center trials, used when the study involves multiple research sites
2. Equipment Provision: Terms regarding equipment provided by sponsor, included when sponsor provides specific equipment for the trial
3. Biological Samples: Provisions for handling biological samples, included when trial involves sample collection and storage
4. Third Party Agreements: Terms regarding subcontractors or other third parties, included when external parties are involved
5. Post-Trial Access: Provisions for post-trial access to study drug, included for certain drug trials
6. Emergency Procedures: Special procedures for emergencies, included for high-risk trials
7. Quality Assurance: Additional quality control measures, included for complex trials or at sponsor's request
1. Schedule A - Protocol: Full clinical trial protocol or protocol summary
2. Schedule B - Budget and Payment Schedule: Detailed financial terms, payment amounts, and timing
3. Schedule C - Timeline: Detailed study timeline and milestones
4. Schedule D - Required Reports: List and templates of required reports and notifications
5. Schedule E - Data Processing Agreement: GDPR-compliant data processing terms and procedures
6. Schedule F - Insurance Certificates: Copies of required insurance certificates
7. Schedule G - Form of Informed Consent: Approved informed consent forms and process
8. Schedule H - Confidentiality Agreement: Detailed confidentiality terms and procedures
9. Schedule I - Equipment List: List and specifications of provided equipment (if applicable)
Authors
Pharmaceuticals
Healthcare
Biotechnology
Medical Devices
Clinical Research
Academic Research
Healthcare Technology
Life Sciences
Contract Research Services
Legal
Clinical Operations
Regulatory Affairs
Research & Development
Medical Affairs
Compliance
Data Protection
Quality Assurance
Clinical Research
Contract Management
Finance
Ethics Committee
Clinical Research Director
Legal Counsel
Regulatory Affairs Manager
Principal Investigator
Clinical Operations Manager
Research Coordinator
Medical Director
Compliance Officer
Data Protection Officer
Contract Manager
Clinical Trial Manager
Chief Medical Officer
Research Site Manager
Clinical Research Associate
Quality Assurance Manager
Find the exact document you need
Clinical Trial Agreement
A German law-governed agreement establishing the framework for conducting clinical trials, ensuring compliance with German and EU regulations.
Clinical Site Agreement
A German law-governed agreement establishing terms for conducting clinical trials at medical institutions, complying with EU and German regulatory requirements.
Clinical Research Agreement
A German law-governed agreement establishing terms and conditions for conducting clinical research studies in Germany, ensuring compliance with local and EU regulations.
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