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Manufacturing Under License Agreement
"I need a Manufacturing Under License Agreement for allowing a Swiss manufacturer to produce our patented medical devices, with exclusive rights in the EU market and strict quality control requirements, starting from March 2025."
1. Parties: Identification of licensor and licensee with full legal details
2. Background: Context of the agreement, including description of the licensed IP and manufacturing purpose
3. Definitions: Definitions of key terms used throughout the agreement
4. Grant of License: Scope of manufacturing license, territory, and any restrictions
5. Manufacturing Requirements: Production specifications, quality standards, and manufacturing location requirements
6. Quality Control: Quality assurance procedures, testing requirements, and inspection rights
7. Intellectual Property Rights: IP ownership, protection obligations, and improvements
8. Confidentiality: Protection of trade secrets and confidential information
9. Commercial Terms: Royalties, payment terms, and reporting requirements
10. Representations and Warranties: Parties' warranties regarding IP rights, manufacturing capabilities, and regulatory compliance
11. Liability and Indemnification: Allocation of risks and indemnification obligations
12. Term and Termination: Duration, renewal terms, and termination rights
13. Post-Termination Obligations: Rights and obligations after agreement ends
14. General Provisions: Standard clauses including governing law, dispute resolution, and entire agreement
1. Exclusivity Provisions: Used when granting exclusive manufacturing rights in specific territories
2. Technology Transfer: Include when technical assistance and know-how transfer is required for manufacturing
3. Raw Materials Supply: Include when specific requirements exist for sourcing of raw materials or components
4. Export Controls: Required when products are subject to export restrictions or controls
5. Minimum Performance Requirements: Include when setting minimum production or sales targets
6. Environmental Compliance: Detailed section when manufacturing involves significant environmental considerations
7. Training and Support: Include when ongoing technical support or training is part of the agreement
8. Sub-manufacturing Rights: Used when sub-licensing or sub-contracting manufacturing is permitted
1. Schedule 1 - Licensed IP: Detailed description of patents, know-how, and other IP being licensed
2. Schedule 2 - Technical Specifications: Detailed manufacturing specifications and technical requirements
3. Schedule 3 - Quality Standards: Quality control procedures, acceptance criteria, and testing methods
4. Schedule 4 - Commercial Terms: Detailed royalty calculations, payment terms, and reporting templates
5. Schedule 5 - Approved Manufacturing Facilities: List of approved manufacturing locations and facility requirements
6. Schedule 6 - Required Approvals: List of regulatory approvals and certifications required
7. Appendix A - Quality Control Procedures: Detailed quality control and testing procedures
8. Appendix B - Reporting Templates: Templates for production reports, royalty calculations, and other required reporting
Authors
Manufacturing
Pharmaceuticals
Biotechnology
Electronics
Automotive
Consumer Goods
Industrial Equipment
Medical Devices
Chemical Industry
Aerospace
Technology Hardware
Legal
Operations
Manufacturing
Quality Control
Research & Development
Intellectual Property
Commercial
Technical Operations
Compliance
Procurement
Chief Technology Officer
Head of Manufacturing
IP Counsel
Quality Control Manager
Production Director
Legal Counsel
Chief Operations Officer
Licensing Manager
Commercial Director
Head of R&D
Procurement Manager
Compliance Officer
Technical Director
Contract Manager
Find the exact document you need
Manufacturing Under License Agreement
Swiss law-governed agreement authorizing manufacturing rights under license, including quality standards, technical specifications, and royalty terms.
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