---
title: "TB-500 COA"
id: "263"
type: "wpdmpro"
slug: "tb-500-coa"
published_at: "2026-06-25T05:57:37+00:00"
modified_at: "2026-06-26T09:48:16+00:00"
url: "https://rplpeptides.com/download/tb-500-coa/"
markdown_url: "https://rplpeptides.com/download/tb-500-coa.md"
excerpt: "Certificate of Analysis (COA) – TB500 – Batch 202605 GO TO TB-500 This Certificate of Analysis (COA) documents the analytical verification of TB500 Batch 202605. All testing was performed under laboratory quality control conditions, including third-party analytical validation by SENO..."
---

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- Create Date June 25, 2026
- Last Updated June 26, 2026

# TB-500 COA

# Certificate of Analysis (COA) – TB500 – Batch 202605

[GO TO TB-500](https://rplpeptides.com/tb-500-peptide-thymosin-beta-4-fragment/)

This Certificate of Analysis (COA) documents the analytical verification of TB500 Batch 202605. All testing was performed under laboratory quality control conditions, including third-party analytical validation by **SENO Test Center**. The report supports batch traceability, laboratory documentation, and research-grade material verification.

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## Overview

TB500 Batch 202605 is a research-grade biochemical reagent analyzed under standardized laboratory conditions. Analytical validation includes HPLC purity testing, LC-MS identity confirmation, and third-party verification performed by SENO Test Center. The COA provides batch-level traceability and quality control documentation for laboratory research use.

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## Batch Information (Structured Record)

| Field | Value |
| --- | --- |
| Product Name | TB500 |
| Batch ID | 202605 |
| Brand | RPL Peptide |
| Category | Research Peptide / Biochemical Research Reagent |
| Production Status | Released for Laboratory Distribution |
| Quality Status | Passed Internal QC + Third-Party Validation |
| Third-Party Testing | SENO Test Center |
| Intended Use | Laboratory Research Use Only |
| COA ID | COA-TB500-202605 |

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## Analytical Verification Summary

Analytical testing is performed using validated laboratory methods. Results are reviewed under internal QC protocols and confirmed via third-party analytical verification.

| Test | Method | Instrument / Validator | Result | Status |
| --- | --- | --- | --- | --- |
| Purity Analysis | HPLC | Internal QC Lab | ≥98.0% | Pass |
| Identity Confirmation | LC-MS | Internal QC Lab | Consistent with Reference Standard | Pass |
| Chromatographic Profile | UPLC | Internal QC Lab | Within Specification | Pass |
| Third-Party Validation | Cross Verification | SENO Test Center | Confirmed Analytical Consistency | Pass |
| Final QC Review | Batch Release Audit | RPL QC System | Approved | Released |

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## Quality Control & Validation System (EEAT Upgrade)

The TB500 COA system operates under a structured quality control workflow that includes internal laboratory testing, batch-level documentation review, and third-party analytical validation performed by SENO Test Center.

Each batch undergoes standardized release procedures including raw data review, chromatographic verification, identity confirmation, and documentation audit prior to release into distribution.

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## Batch Traceability System

Each production batch is assigned a unique identifier that connects manufacturing records, analytical results, QC review logs, and third-party validation reports. This system ensures full traceability from production to final COA issuance.

Batch 202605 is linked to internal QC records and external validation data from SENO Test Center for cross-verification integrity.

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## Certificate of Analysis Documentation

A Certificate of Analysis (COA) is a controlled laboratory document containing batch-specific analytical data, quality control results, and release authorization. It serves as a formal record for laboratory procurement, inventory tracking, and research documentation.

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## Download COA

[Download COA PDF – TB500 Batch 202605](#)
  
 File Size: 2.53 MB | Format: PDF | Updated: June 26, 2026

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## Frequently Asked Questions (FAQ)

### What is a Certificate of Analysis (COA)?

A COA is a laboratory document that provides batch-specific analytical results and quality control verification for research materials.

### What does SENO Test Center do in this COA?

SENO Test Center provides third-party analytical validation to confirm consistency of internal laboratory results.

### Which methods are used for analysis?

Standard methods include HPLC for purity, LC-MS for identity confirmation, and UPLC for chromatographic profiling.

### Is batch-specific data available?

Yes, all COA data is generated per batch and linked to a unique batch identifier.

### What is batch traceability?

Batch traceability refers to the system that connects production records, analytical data, and QC documentation for each batch.

### Is this material for human use?

No. This product is strictly intended for laboratory research use only.

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