QA METHODOLOGY
The rules every batch is held to.
Our HPLC-MS workflow, batch-traceability rules, and CoA anatomy — written out so Australian labs can audit our process before they trust the vial.
RESEARCH LEARNING PATH
CORE PRINCIPLES
Our Research Standards Are Built On
Four core principles that govern everything we do.
Documentation First
Every material is referenced with batch-level documentation and traceability.
Independent Verification
Where applicable, materials are supported by third-party analytical testing records.
Batch Transparency
Materials are identified and referenced by batch, not marketing descriptions.
Responsible Positioning
No medical, therapeutic, or performance claims are made.
DOCUMENTATION
What Is a Certificate of Analysis (COA)?
A Certificate of Analysis (COA) is a laboratory document summarising analytical testing performed on a specific material batch.
COAs may include:
- • Purity analysis
- • Batch identifiers
- • Analytical methodology (e.g. HPLC)
- • Verification timestamps
A COA is a reference document, not a claim of suitability for any particular application. Researchers are responsible for determining appropriate use within their laboratory context.
GUIDE
How to Read a COA
Understanding the key components of analytical documentation.
Batch Identifier
A unique alphanumeric code assigned to a specific production batch for traceability.
Purity Result (%)
The percentage purity of the analyzed material — the proportion of target compound detected.
Analytical Method
The laboratory technique used (e.g., HPLC, HPLC-MS). Different methods yield varying specificity.
Test Date
The date analytical testing was performed, providing context for documentation currency.
Laboratory / Verification Source
Information about the facility or organization that conducted the testing.
Verification Timestamp
A digital timestamp confirming when the document was generated or validated.
PROCESS
Verification & Traceability Process
Our four-step approach to material documentation.
Batch Identification
Each material is assigned a unique batch identifier for tracking and documentation.
Documentation Collection
Relevant analytical documentation is collected and associated with the specific batch.
Internal Completeness Review
Documentation is reviewed internally for completeness and consistency with batch specifications.
Public Documentation Access
Where applicable, documentation is made available for independent researcher review.
GUIDELINES
Handling & Storage Guidelines
Proper handling and storage practices for maintaining material integrity.
Controlled Temperature Storage
Materials should be stored at appropriate temperatures as indicated in documentation.
Proper Labelling
All materials should be clearly labelled with batch identifiers and storage requirements.
Documentation Retention
All associated documentation should be retained and accessible for research reference.
Batch Separation
Different batches should be stored separately to maintain traceability and prevent cross-contamination.
Documentation & Verification FAQs
Common questions about analytical documentation and quality processes.
What We Do Not Do
We maintain clear boundaries to ensure responsible positioning of research materials:
- Provide medical advice
- Make therapeutic or performance claims
- Promote human or veterinary use
- Offer dosage or administration guidance