Written procedures
Every recurring activity has a written procedure with a version, an owner and a review date.
Quality
Documentation is the experiment.
A result that cannot be traced back to its record is not a result. Our quality framework exists so that every statement we make can be followed to its source.
Batch identity
Each batch carries a unique code that links it to its preparation record, analytical data and storage history.
Retained records
Documentation is retained and archived so any result can be reconstructed from source records.
Independent review
A second reader reviews analytical conclusions before they are recorded as final.
Controlled storage
Materials are stored under defined conditions with monitored, logged environments.
Clear scope
We state plainly what a record does and does not establish, and avoid claims beyond the data.
Documentation library
Everything traceable, in one place.
The documentation library is being prepared. As records are released they will appear here and in the researcher portal, organized by category.
Batch information
Awaiting release
Certificates of Analysis
Awaiting release
Testing documentation
Awaiting release
Product specifications
Awaiting release
Research documentation
Awaiting release
Handling & storage records
Awaiting release
Responsible research
What we do not claim.
Restraint is part of the standard. We describe research materials and documentation, and we stop there.
- We make no medical, therapeutic, diagnostic or disease-treatment claims.
- Nothing we document is intended for human or veterinary use, or for consumption.
- We do not describe outcomes we have not measured, and we do not extrapolate beyond the conditions tested.
- Access to detailed records is limited to verified researchers working in appropriate laboratory settings.