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Share your intended use and whether any third parties are involved. We will recommend the most appropriate agreement and help keep your project moving without delays.
Product Use Policy
This overview explains what is typically permitted under Cytion’s standard research MTA and when a separate commercial or project-specific agreement is required. The binding terms are defined in the applicable agreement.
Section A
Standard Research MTA
Designed for internal research and development across academic and commercial organisations when work is conducted for their own R&D.
Permitted under the standard MTA
- Internal research and development
- Use within your organisation, including multi-site and affiliated entities (as covered by the MTA)
- Generation of research data, results, and Modifications
- Defined non-commercial collaborations
- Third-party testing labs for identity, quality, or safety testing (as service providers)
Not covered (separate agreement required)
- Commercial or fee-for-service research performed for third parties
- Clinical or regulatory studies and pre-market testing
- Manufacturing, scale-up, batch release, potency, or viral clearance
- Commercial distribution, licensing, or transfer for consideration
Section B
Commercial or Extended-Use Agreements
For projects involving commercial services, regulated development, manufacturing, or any intended use beyond internal R&D.
Typical scenarios
- CRO/CDMO work for third parties or client-sponsored projects
- Commercial development, validation, or regulated workflows
- Manufacturing, scale-up, or product/batch release
- Clinical, diagnostic, or pre-market studies
How it works
- Tell us the intended use, parties involved, and scope
- We propose a project-specific agreement aligned to your workflow
- Clear documentation and defined rights to keep projects moving
Quick Comparison
Use this overview to determine whether the standard research MTA is sufficient for your project scope.
| Use case | Standard Research MTA | Commercial Agreement |
|---|---|---|
| Internal research and development | Yes | Yes |
| Non-commercial collaborations (defined project scope) | Yes | Yes |
| Third-party testing labs (identity, quality, safety) | Yes | Yes |
| Multi-site or affiliate use (within your organisation) | Yes | Yes |
| CRO/CDMO involvement for commercial projects | Separate agreement | Yes |
| Clinical, regulatory, or pre-market studies | Separate agreement | Yes |
| Manufacturing, scale-up, batch release, potency, viral clearance | Separate agreement | Yes |
| Commercial services or fee-for-service projects | Separate agreement | Yes |
This page is provided for convenience only. The applicable agreement governs in all cases.
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