Quality scoped to what a material has actually demonstrated.
TruBiotech develops materials at varying levels of maturity. Quality, characterisation and documentation are matched to each material's development stage rather than described as blanket capabilities.
Methods matched to material class.
Identity, purity and consistency assessments are selected per material — peptide fractions, microbial polysaccharides, bioconverted botanicals and functional materials each require different analytical approaches.
Assessed across development batches.
Compositional and functional consistency is tracked across development batches as a material progresses toward pilot stage.
Issued when it can be substantiated.
Technical data sheets, specifications and supporting documentation are provided on request per material and reflect the current state of that material's development.
Confirmed on a per-project basis.
Regulatory suitability for a specific finished product is scoped in discussion with the customer, and depends on formulation architecture, market and intended claims.
Request documentation against a specific material.
Documentation status is displayed on each ingredient profile. Use the Technical Request to consolidate documentation requests across multiple materials.