RESEARCH PEPTIDE QUALITY STANDARDS NZ
The rules every batch is held to.
Our HPLC-MS workflow, batch-traceability rules, and COA anatomy — written out so New Zealand research teams can audit the KP-99 Purity Standard before they trust the vial.
RESEARCH LEARNING PATH
CORE PRINCIPLES
The KP-99 Purity Standard is built on four rules
Four principles that govern everything we do in New Zealand.
Documentation First
Every reference material carries batch-level documentation and traceability inside The Batch Book.
Independent Verification
Materials are backed by third-party HPLC-MS analytical testing, not in-house sign-off.
Batch Transparency
Materials are identified and referenced by batch number, never by marketing description.
Responsible Positioning
No medical, therapeutic, or performance claims are made anywhere on this site.
DOCUMENTATION
What is a Certificate of Analysis (COA)?
A Certificate of Analysis is a laboratory document summarising the analytical testing performed on a specific batch, published inside The Batch Book.
COAs may include:
- • Purity analysis against the KP-99 Purity Standard
- • Batch identifiers
- • Analytical methodology (e.g. HPLC-MS)
- • Verification timestamps
A COA is a reference document, not a claim of suitability for any particular application. Researchers remain responsible for determining appropriate use within their own lab.
GUIDE
How to read a COA
Understanding the key fields in each Batch Book entry.
Batch Identifier
A unique alphanumeric code assigned to a specific New Zealand production batch for traceability.
Purity Result (%)
The measured percentage purity of the batch — the proportion of target compound detected against the KP-99 Purity Standard.
Analytical Method
The laboratory technique used, typically HPLC-MS. Different methods yield different specificity.
Test Date
The date analytical testing was performed, giving context for documentation currency.
Laboratory / Verification Source
Details of the facility that conducted the independent testing.
Verification Timestamp
A digital timestamp confirming when the certificate was generated or validated.
PROCESS
Verification & traceability process
Our four-step approach behind every batch we dispatch across New Zealand.
Batch Identification
Each material is assigned a unique batch identifier for tracking and documentation.
Documentation Collection
Relevant analytical documentation is collected and matched to the specific batch.
Internal Completeness Review
Documentation is reviewed for completeness against the KP-99 Purity Standard before release.
Public Documentation Access
Certificates are published to The Batch Book for independent researcher review.
GUIDELINES
Handling & storage guidelines
Proper handling and storage practices for maintaining material integrity on the bench.
Controlled Temperature Storage
Materials should be stored at the temperature indicated on their batch 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 avoid cross-contamination.
Documentation & verification FAQs
Common questions about The Batch Book and our quality process.
What we do not do
We keep clear boundaries around responsible positioning of research materials:
- Provide medical advice
- Make therapeutic or performance claims
- Promote human or veterinary use
- Offer dosage or administration guidance