红杏直播

Biological Material Transfer Agreement Template for Canada

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

4.6 / 5
4.8 / 5

Let's create your 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聽of your information

Key Requirements PROMPT example:

Biological Material Transfer Agreement

"I need a Biological Material Transfer Agreement for transferring cell lines from our university research lab to a pharmaceutical company for cancer research, with strict confidentiality provisions and publication rights for our researchers."

Document background
The Biological Material Transfer Agreement (MTA) is a critical legal instrument used in Canadian research and commercial contexts to facilitate the controlled transfer of biological materials between organizations. This document becomes necessary whenever biological materials such as cell lines, plasmids, antibodies, or other biological specimens need to be transferred from a providing institution to a recipient for research, evaluation, or commercial development purposes. The agreement ensures compliance with Canadian regulations including the Human Pathogens and Toxins Act, Canadian Biosafety Standards, and relevant provincial requirements. It addresses key aspects such as material handling, biosafety protocols, intellectual property rights, publication permissions, and commercialization restrictions. The MTA is particularly important in maintaining proper documentation and control over valuable research materials while protecting the rights of both providers and recipients under Canadian jurisdiction.
Suggested Sections

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

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

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

4. Material Transfer: Details of the biological materials being transferred, including quantity, form, and shipping arrangements

5. Use of Material: Permitted uses, restrictions, and scope of authorized research

6. Compliance: Requirements for regulatory compliance, biosafety, and handling procedures

7. Intellectual Property: Rights to materials, derivatives, and research results

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

9. Publication: Rights and requirements for publishing research results

10. Warranties and Liability: Disclaimers, warranties, and allocation of risks

11. Term and Termination: Duration of agreement, termination conditions, and post-termination obligations

12. General Provisions: Standard clauses including notices, assignment, governing law, and entire agreement

Optional Sections

1. Commercial Use: Required when there is potential for commercial exploitation of research results

2. Human Biological Materials: Additional provisions required when transferring human specimens or derivatives

3. Export Control: Required for international transfers or materials subject to export restrictions

4. Cost Recovery: Include when the provider charges fees for material preparation and shipping

5. Third Party Rights: Required when materials incorporate third-party components or rights

6. Data Protection: Required when personal data is associated with biological materials

7. Return or Destruction: Specific requirements for material disposition after project completion

Suggested Schedules

1. Schedule A - Material Description: Detailed technical description of the biological materials, including source, characterization, and quantity

2. Schedule B - Research Plan: Description of the intended research, methodology, and objectives

3. Schedule C - Biosafety Requirements: Specific handling, containment, and safety procedures required for the materials

4. Schedule D - Fee Schedule: Breakdown of any applicable fees for material preparation and transfer

5. Schedule E - Contact Information: Detailed contact information for key personnel and authorized representatives

6. Appendix 1 - Shipping Instructions: Detailed protocols for packaging, labeling, and shipping the materials

7. Appendix 2 - Required Permits: Copies or details of required permits, certifications, or authorizations

Authors

Alex Denne

Head of Growth (Open Source Law) @ 红杏直播 | 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

Healthcare

Pharmaceuticals

Academic Research

Medical Research

Agriculture

Environmental Science

Clinical Research

Life Sciences

Public Health

Relevant Teams

Legal

Research and Development

Regulatory Affairs

Technology Transfer Office

Laboratory Operations

Quality Assurance

Research Administration

Compliance

Intellectual Property

Scientific Operations

Relevant Roles

Research Director

Laboratory Manager

Principal Investigator

Technology Transfer Officer

Legal Counsel

Biosafety Officer

Research Compliance Manager

Scientific Director

Intellectual Property Manager

Research Administrator

Quality Assurance Manager

Regulatory Affairs Specialist

Contract Manager

Research Scientist

Laboratory Supervisor

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, 聽Leaves of Absence, Confidentiality, Intellectual Property, Non-Solicitation, Non-Competition, Code of Conduct, Termination, 聽Severance Pay, Governing Law, Entire Agreemen

Find the exact document you need

Material Transfer Form

A Canadian-compliant legal document governing the transfer of materials between organizations, establishing terms, conditions, and compliance requirements under Canadian law.

find out more

Material Transfer Agreement

A Canadian-law governed agreement for the transfer of research materials between organizations, establishing terms for material use, handling, and associated rights.

find out more

Data Transfer Agreement Clinical Trial

Canadian-law governed agreement for transferring clinical trial data between parties, ensuring compliance with privacy and clinical trial regulations.

find out more

Biological Material Transfer Agreement

A Canadian-law governed agreement for the transfer of biological materials between organizations, establishing usage terms and compliance requirements.

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.

骋别苍颈别鈥檚 Security Promise

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

Your documents are private:

We do not train on your data; 骋别苍颈别鈥檚 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 拢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.