01 / CUSTOMER
Asset concept
Clinical need • indication • product concept • commercial opportunity

Maverick develops proprietary biomaterial technologies, then manufactures them for partners or licenses them for further development, all built on our materials and processing expertise.

We manufacture the product for you using the same controlled source and processes established during development.
Processing & Manufacturing

Acquire or license a preclinical technology and take it through development, regulatory approval and commercialisation.
Talk to our team
Each technology moves through a defined development pathway, turning an early concept into a characterised, preclinical-ready product supported by the evidence needed for what comes next.

A clinical need, a defined indication and a product concept with commercial potential.

Material selection, formulation, process development and analytical strategy.

A characterised product made under controlled conditions, with defined specifications and traceability.

Safety, performance and technical evidence that prepares the technology for its next stage.
How an asset progresses from concept to preclinical validation, licensing and commercialisation.
01 / CUSTOMER
Clinical need • indication • product concept • commercial opportunity
02 / CDO / CDMO
Material selection • formulation • process development • analytical strategy
03 / CDO / CDMO
Characterised product • controlled manufacture • specifications • traceability
04 / PRECLINICAL VALIDATION
Biocompatibility • toxicology • GLP studies where required
Proof of concept • efficacy • functional performance
Characterisation • stability • manufacturing controls
05 / CUSTOMER
IP position • data room • development plan • regulatory pathway • commercial proposition
06 / LICENSING PARTNER
Technology • IP • preclinical evidence • CMC • regulatory pathway • scalability
07 / TRANSLATION
Partner advances the asset with CDO / CDMO support for tech transfer, scale-up and manufacturing.
Every ODM program draws on the same foundation: source control, scientific and processing expertise, certified quality systems and a path to commercial manufacture.

Australian and New Zealand origin materials, selected, controlled and traced from the source.

ISO 13485 and ISO 9001 certified, with controlled cleanroom manufacturing.

Advanced processing backed by expertise across ECM biology, collagen biomaterials and 3D bioprinting.

The same controlled sources and processes can support development through commercial manufacture.
Tell us about the clinical need or product area you are exploring, and we’ll show you where Maverick’s technologies could fit.z