tiktok³ÉÈ˰æ

Uniform Biological Material Transfer Agreement Template for Netherlands

Create a bespoke document in minutes,  or upload and review your own.

4.6 / 5
4.8 / 5

Let's create your Uniform Biological Material Transfer Agreement

Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.

Get your first 2 documents free

Your data doesn't train Genie's AI

You keep IP ownership of your information

Key Requirements PROMPT example:

Uniform Biological Material Transfer Agreement

"I need a Uniform Biological Material Transfer Agreement for transferring stem cell lines from our university laboratory in Amsterdam to a research institution in Utrecht, with strict confidentiality provisions and a requirement that any research publications acknowledge our lab's contribution."

Document background
The Uniform Biological Material Transfer Agreement (UBMTA) is a fundamental legal instrument used in the Netherlands for facilitating the transfer of biological materials between organizations. This standardized agreement is designed to comply with Dutch legal requirements while incorporating relevant EU regulations and international protocols. It is particularly crucial when research institutions, universities, or commercial entities need to transfer biological materials for research purposes. The document includes comprehensive provisions for material handling, intellectual property rights, safety protocols, and regulatory compliance. The UBMTA helps streamline the transfer process while ensuring all parties understand their rights and obligations under Dutch law, particularly in relation to the Nagoya Protocol, GMO regulations, and biodiversity conservation requirements. This agreement is essential for maintaining proper documentation and ensuring compliance with both national and international standards for biological material transfer.
Suggested Sections

1. Parties: Identification of the Provider and Recipient institutions and their authorized representatives

2. Background: Context of the material transfer and the research purpose

3. Definitions: Definitions of key terms including 'Material', 'Progeny', 'Unmodified Derivatives', 'Modifications', and 'Commercial Purposes'

4. Scope of Agreement: Overview of what is being transferred and the permitted uses

5. Provider's Rights and Obligations: Rights retained by the Provider and their obligations regarding the material transfer

6. Recipient's Rights and Obligations: Rights granted to the Recipient and their obligations regarding material use and storage

7. Use of Materials: Specific terms governing how the materials may be used, including research limitations

8. Confidentiality: Provisions regarding confidential information related to the materials

9. Intellectual Property: Handling of IP rights related to the materials and any discoveries

10. Publications: Terms governing the publication of research results using the materials

11. Warranties and Indemnification: Disclaimers, warranties, and indemnification provisions

12. Term and Termination: Duration of the agreement and conditions for termination

13. Post-Termination Obligations: Obligations that survive termination of the agreement

14. Governing Law and Jurisdiction: Specification of Dutch law as governing law and jurisdiction

15. Execution: Signature blocks and execution details

Optional Sections

1. Cost and Shipping: Include when there are specific costs or shipping requirements for the material transfer

2. Third Party Rights: Include when the materials involve third-party rights or restrictions

3. Export Control: Include when materials are subject to export control regulations

4. Data Protection: Include when personal data or sensitive research data is involved

5. Biosafety Requirements: Include when materials require specific biosafety handling procedures

6. Commercial Development: Include when there's potential for commercial development of research results

7. Return of Results: Include when the Provider requires sharing of research results

8. Material Tracking: Include when specific tracking or reporting of material use is required

9. Nagoya Protocol Compliance: Include when materials fall under Nagoya Protocol requirements

Suggested Schedules

1. Schedule A - Material Description: Detailed description of the biological materials being transferred

2. Schedule B - Research Plan: Detailed description of the intended research using the materials

3. Schedule C - Material Handling Protocols: Specific protocols for handling, storage, and disposal of materials

4. Schedule D - Fee Schedule: Details of any fees associated with the material transfer

5. Appendix 1 - Safety Data Sheet: Safety information and handling requirements for the materials

6. Appendix 2 - Authorized Users: List of authorized personnel who may access and use the materials

7. Appendix 3 - Required Permits: Copies of relevant permits and authorizations

8. Appendix 4 - Transfer Documentation: Shipping and transfer documentation requirements

Authors

Alex Denne

Head of Growth (Open Source Law) @ tiktok³ÉÈ˰æ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

Relevant legal definitions





























Clauses




































Relevant Industries

Biotechnology

Pharmaceuticals

Academic Research

Healthcare

Life Sciences

Agricultural Science

Medical Research

Environmental Science

Chemical Industry

Public Health

Relevant Teams

Legal

Research & Development

Compliance

Regulatory Affairs

Laboratory Operations

Technology Transfer

Quality Assurance

Scientific Affairs

Contract Administration

Intellectual Property

Research Ethics

Biosafety

Relevant Roles

Research Director

Legal Counsel

Compliance Officer

Laboratory Manager

Principal Investigator

Technology Transfer Officer

Biosafety Officer

Research Scientist

Regulatory Affairs Manager

Material Transfer Agreement Coordinator

IP Manager

Quality Assurance Manager

Research Ethics Officer

Scientific Director

Contract Manager

Industries










Teams

Employer, Employee, Start Date, Job Title, Department, Location, Probationary Period, Notice Period, Salary, Overtime, Vacation Pay, Statutory Holidays, Benefits, Bonus, Expenses, Working Hours, Rest Breaks,  Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination,  Severance Pay, Governing Law, Entire Agreemen

Find the exact document you need

Subaward Agreement

A Dutch law-governed agreement transferring partial project rights and obligations from a primary award recipient to a subawardee, including terms for project execution, financial management, and compliance requirements.

find out more

Research Participant Confidentiality Agreement

Dutch law-governed confidentiality agreement between research institutions and study participants, ensuring data protection and research integrity under EU and Dutch regulations.

find out more

Uniform Biological Material Transfer Agreement

A Dutch law-governed agreement for the standardized transfer of biological materials between organizations, incorporating EU and Dutch regulatory requirements.

find out more

Research Funding Agreement

Dutch law-governed agreement establishing terms for research funding between funding bodies and research institutions.

find out more

Research Cooperation Agreement

Dutch law-governed agreement establishing terms and conditions for collaborative research activities between multiple parties, including IP rights, confidentiality, and operational framework.

find out more

Research Contract

A Dutch law-governed agreement establishing terms and conditions for conducting research activities, including IP rights, data protection, and research obligations.

find out more

Standard Research Agreement

Dutch law-governed agreement establishing terms and conditions for collaborative research activities between parties, including IP rights, funding, and research obligations.

find out more

Sponsored Research Agreement

A Dutch law-governed agreement establishing terms for sponsored research collaboration between a research institution and funding entity.

find out more

Research Service Agreement

Dutch law-governed agreement for research services, defining scope, IP rights, and obligations between research provider and client.

find out more

Research License Agreement

A Dutch law agreement governing the license of intellectual property or materials for research purposes, including terms for usage, IP rights, and compliance requirements.

find out more

Data Use Agreement

A Dutch law-governed agreement establishing terms for data sharing and processing, ensuring GDPR compliance and data protection.

find out more

Studentship Agreement

A Dutch law-governed agreement between an educational institution and student, establishing terms and conditions of studentship in the Netherlands.

find out more

Research Data Sharing Agreement

Dutch-law agreement governing the sharing of research data between organizations, ensuring GDPR compliance and research integrity.

find out more

Investigator Agreement

A Dutch-law governed agreement between a sponsor/institution and an investigator for conducting clinical research, complying with WMO and GDPR requirements.

find out more

Interview Consent Agreement

Dutch law-compliant interview consent agreement covering data protection, usage rights, and GDPR requirements for conducting and utilizing interview content.

find out more

Biobank Agreement

Dutch law-governed agreement for managing biobank operations, including sample collection, storage, and data handling under EU and Dutch regulations.

find out more

Project Transfer Agreement

A Dutch law-governed agreement facilitating the comprehensive transfer of project rights, obligations, and responsibilities between entities.

find out more

Clinical Trial Contract

A Dutch law-governed agreement for conducting clinical trials, establishing terms between sponsors, research institutions, and investigators while ensuring compliance with Netherlands and EU regulations.

find out more

Joint Research And Development Agreement

Dutch law-governed agreement establishing terms for collaborative R&D activities between multiple parties, including IP rights, resource allocation, and research scope.

find out more

Indirect Cost Agreement

Dutch law agreement establishing framework for allocation of indirect costs between entities, including methodology and compliance requirements.

find out more

Technology Development Agreement

Dutch law-governed agreement for custom technology development, outlining development scope, IP rights, and delivery terms.

find out more

Research Grant Agreement

A Dutch law-governed agreement establishing terms and conditions for research funding between a grant-giving organization and recipient institution.

find out more

Clinical Trial Confidentiality Agreement

A Dutch law-governed confidentiality agreement for protecting sensitive information in clinical trials, compliant with EU and Dutch medical research regulations.

find out more

Biological Material Transfer Agreement

Dutch law-governed agreement for the transfer of biological materials between organizations, incorporating EU regulations and international protocols.

find out more

Clinical Study Agreement

Dutch law-governed agreement for conducting clinical research studies, compliant with Netherlands and EU regulations for medical research and data protection.

find out more

Technology Transfer Agreement

Dutch law-governed agreement for transferring technology and associated IP rights between parties, compliant with EU regulations.

find out more

Contract Research Agreement

Dutch law agreement governing collaborative research activities, including IP rights, confidentiality, and research terms.

find out more

Collaboration Research Agreement

A Dutch law-governed agreement establishing terms and conditions for joint research activities between multiple parties, including IP rights, confidentiality, and project management provisions.

find out more

Download our whitepaper on the future of AI in Legal

By providing your email address you are consenting to our Privacy Notice.
Thank you for downloading our whitepaper. This should arrive in your inbox shortly. In the meantime, why not jump straight to a section that interests you here: /our-research
Oops! Something went wrong while submitting the form.

³Ò±ð²Ô¾±±ð’s Security Promise

Genie is the safest place to draft. Here’s how we prioritise your privacy and security.

Your documents are private:

We do not train on your data; ³Ò±ð²Ô¾±±ð’s AI improves independently

All data stored on Genie is private to your organisation

Your documents are protected:

Your documents are protected by ultra-secure 256-bit encryption

Our bank-grade security infrastructure undergoes regular external audits

We are ISO27001 certified, so your data is secure

Organizational security

You retain IP ownership of your documents

You have full control over your data and who gets to see it

Innovation in privacy:

Genie partnered with the Computational Privacy Department at Imperial College London

Together, we ran a £1 million research project on privacy and anonymity in legal contracts

Want to know more?

Visit our for more details and real-time security updates.