PEPTINOVA

Peptide manufacturing

Precision forevery peptideprogram.

A focused manufacturing partner for international research, development and procurement teams.

Company Introduction

Peptide manufacturing, shaped around precision and clear collaboration.

0+Years of Expertise
0+ m²Manufacturing Facility
0+ kgAnnual Peptide Capacity
0+Employees

A focused manufacturing partner for international research, development and procurement teams.

We bring technical requirements, manufacturing planning and quality documentation into one clear conversation. Final company claims will be published only after verification.

Learn About Our Company

Manufacturing focus

Precision begins with the environment.

Manufacturing

A controlled path through production.

01

Peptide Synthesis

The peptide chain is assembled step by step according to the target amino acid sequence, typically using solid-phase peptide synthesis (SPPS).

Technician operating automated peptide synthesis equipment
02

Cleavage & Deprotection

After synthesis, the peptide is cleaved from the resin support and protective groups are removed to obtain the crude peptide.

Blue-gloved hand handling a peptide sample vial near laboratory equipment
03

Purification

Preparative HPLC and other purification techniques are used to separate the target peptide from impurities and improve overall purity.

Cleanroom technicians reviewing peptide purification equipment and analytical data
04

Concentration & Lyophilization

The purified peptide solution is concentrated and freeze-dried into a stable powder for easier storage and further processing.

Gloved hands inspecting a clear vial in a controlled laboratory
05

Analytical Testing

Analytical methods such as HPLC and LC-MS are used to verify purity, molecular weight, content, and other key quality parameters.

HPLC analytical workstation with chromatogram display and laboratory technician
06

Filling & Quality Release

Qualified peptide products are filled, packaged, documented by batch, and released after final quality review.

Automated stainless steel filling line processing clear glass vials

Quality standards

Standards and testing capabilities are presented as replaceable fields. A label does not indicate certification until supporting documents have been approved.

Certificate of Analysis

Reta30

01 / 09
Reta30 Certificate of Analysis
01

GMP

Manufacturing processes are designed around GMP-aligned quality principles, with controlled procedures, documented workflows, and quality oversight across production activities.

02

ISO

Quality management practices are structured with reference to applicable ISO standards, supporting consistency, documentation, and continuous process improvement.

03

HPLC

High-performance liquid chromatography is used to evaluate peptide purity, identify related impurities, and support batch-level analytical assessment.

04

MS Testing

Mass spectrometry supports molecular weight confirmation and peptide identity verification, providing an additional layer of analytical confidence.

05

COA

Each qualified batch can be supported by a Certificate of Analysis summarizing key analytical results, specifications, and relevant quality parameters.

06

Batch Traceability

Production records are maintained throughout the manufacturing workflow, enabling traceability from raw materials and processing steps through final batch release.

Peptide Manufacturing | PEPTINOVA