tiktok³ÉÈË°æ

All Countries
Material Transfer Agreement

Material Transfer Agreement Template for New Zealand

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

4.6 / 5
4.8 / 5

Let's create your 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:

Material Transfer Agreement

"I need a Material Transfer Agreement for transferring biological research samples from our university lab to a commercial biotechnology company in Auckland, with specific provisions for maintaining confidentiality and restricting use to non-commercial research purposes until March 2025."

Celebrated by
Collaborations with
Investors
Document background
The Material Transfer Agreement (MTA) is a specialized legal instrument used when one organization (the Provider) transfers tangible research materials to another organization (the Recipient) for research purposes. This agreement type is essential in New Zealand's research and development landscape, particularly where valuable biological, chemical, or physical materials are shared between institutions. The document must comply with New Zealand's specific regulatory framework, including the Hazardous Substances and New Organisms Act 1996, Treaty of Waitangi obligations, and biosecurity requirements. MTAs are crucial for protecting intellectual property rights, ensuring appropriate use of materials, maintaining confidentiality, and establishing clear parameters for research activities. They are particularly important in collaborative research projects, academic-industry partnerships, and international research initiatives.
Suggested Sections

1. Parties: Identification and details of the Provider and Recipient organizations

2. Background: Context of the transfer, relationship between parties, and purpose of the agreement

3. Definitions: Definitions of key terms including 'Materials', 'Derivatives', 'Research Purpose', and other technical terms

4. Supply of Materials: Details of what materials will be provided, quantity, quality, and timing of transfer

5. Permitted Use: Specific permitted uses of the materials, including research scope and limitations

6. Title and Intellectual Property: Ownership of materials, existing IP rights, and rights to new discoveries or developments

7. Confidentiality: Obligations regarding confidential information related to the materials and research

8. Publication Rights: Terms governing the publication of research results using the materials

9. Warranties and Liability: Disclaimers, warranties, and allocation of risks related to the materials

10. Term and Termination: Duration of the agreement and circumstances for termination

11. Post-Termination Obligations: Requirements after agreement ends, including return or destruction of materials

12. General Provisions: Standard legal provisions including governing law, dispute resolution, and entire agreement

Optional Sections

1. Cost and Payment: Include when there are charges for materials or shipping

2. Safety Precautions: Required for hazardous materials or those requiring special handling

3. Regulatory Compliance: Include for materials subject to specific regulations or requiring permits

4. Third Party Rights: Necessary when materials involve third-party intellectual property rights

5. Export Control: Include for international transfers subject to export regulations

6. Traditional Knowledge: Required when materials involve indigenous resources or knowledge

7. Commercial Use Restrictions: Include specific provisions prohibiting commercial use when required

8. Reporting Requirements: Include when regular updates on material use are required

Suggested Schedules

1. Schedule 1 - Description of Materials: Detailed technical description of materials being transferred

2. Schedule 2 - Transfer Protocol: Specific procedures for handling, shipping, and receiving materials

3. Schedule 3 - Research Plan: Detailed description of intended research using the materials

4. Schedule 4 - Safety Data: Safety information and handling requirements for hazardous materials

5. Schedule 5 - Authorized Users: List of authorized personnel who may access and use the materials

6. Appendix A - Required Permits: Copies of relevant permits and regulatory approvals

7. Appendix B - Material Safety Data Sheets: Detailed safety information for hazardous materials

Authors

Alex Denne

Head of Growth (Open Source Law) @ tiktok³ÉÈË°æ | 3 x UCL-Certified in Contract Law & Drafting | 4+ Years Managing 1M+ Legal Documents | Serial Founder & Legal AI Author

alex.den.21@genieai.co
Relevant legal definitions








































Clauses






























Relevant Industries

Biotechnology

Pharmaceuticals

Healthcare

Academic Research

Agriculture

Chemical Industry

Environmental Science

Medical Research

Life Sciences

Materials Science

Relevant Teams

Legal

Research and Development

Intellectual Property

Compliance and Regulatory Affairs

Laboratory Operations

Technology Transfer

Scientific Affairs

Quality Assurance

Contract Administration

Research Operations

Relevant Roles

Research Director

Legal Counsel

Intellectual Property Manager

Laboratory Manager

Research Scientist

Compliance Officer

Technology Transfer Officer

Principal Investigator

Research Administrator

Biosafety Officer

Contracts Manager

Scientific Director

Quality Assurance Manager

Research Partnership 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

Indirect Rate Agreement

A New Zealand-governed agreement establishing the methodology for calculating and charging indirect costs between parties, ensuring compliance with local accounting and tax regulations.

find out more

Academic Collaboration Agreement

A New Zealand-governed agreement establishing collaboration terms between academic institutions, covering research, resources, and intellectual property.

find out more

Material Transfer Agreement

New Zealand-governed agreement for the transfer of research materials between organizations, addressing ownership, usage rights, and compliance requirements.

find out more

Research Contract

A New Zealand-governed agreement establishing terms and conditions for research activities, including funding, IP rights, and research obligations.

find out more

Sponsored Research Agreement

A New Zealand-governed agreement establishing terms for sponsored research activities between a funding organization and research institution.

find out more

Research Service Agreement

A New Zealand-governed agreement establishing terms and conditions for the provision of research services, including scope, deliverables, and intellectual property rights.

find out more

Data Use Agreement

A New Zealand law-governed agreement establishing terms for data sharing and usage between organizations, ensuring Privacy Act 2020 compliance.

find out more

Investigator Agreement

A New Zealand-governed agreement establishing terms and conditions for conducting clinical or research studies by qualified investigators.

find out more

Confidentiality Agreement For Research Participants

A New Zealand-compliant agreement establishing confidentiality obligations between researchers and study participants, protecting research integrity and participant privacy.

find out more

Clinical Trial Contract

A New Zealand-governed agreement establishing the framework for conducting clinical trials, outlining parties' responsibilities and ensuring regulatory compliance.

find out more

Confidential Disclosure Agreement In Clinical Research

A New Zealand-compliant confidentiality agreement for protecting sensitive information in clinical research activities, aligned with local privacy and healthcare regulations.

find out more

Clinical Study Agreement

A New Zealand-governed agreement establishing the legal framework for conducting clinical research studies, defining responsibilities between sponsors, institutions, and investigators.

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.

Read our Privacy Policy.