Quality & Documentation
Formulation research depends on knowing exactly what a material is, batch to batch. This is how Lyomera approaches documentation and analytical review.
Consistent specifications
Each catalog listing states a defined specification, such as purity, molecular profile or formulation class, so research teams can plan comparable experiments across batches.
Batch-specific documentation
Certificates of analysis and batch information are prepared per production lot and made available on request to support identity and purity review in your own laboratory.
Analytical review
Where applicable, HPLC and mass-spectrometry information supports the stated specification; proprietary liquid formulations are evaluated against their own batch acceptance criteria.
- 01
Specification
A target specification is defined for each catalog material before production or formulation.
- 02
Production / formulation
Peptide synthesis or liquid formulation is carried out to the defined specification.
- 03
Analytical review
Batch samples are reviewed against the specification using the applicable analytical methods.
- 04
Documentation & release
Batch documentation is finalised and made available to research teams on request alongside shipment.