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OEM CONTRACT MANUFACTURING

Defined Specifications.
Controlled Execution.

For organizations that arrive with a clear product vision – we provide the manufacturing infrastructure to realize it precisely.

OUR OPERATING PRINCIPLE

You define the product.
We execute the production.

How the OEM Model Works

Our OEM model is designed for partners who provide defined peptide compounds, dosage parameters, and finished product specifications. We execute manufacturing under a disciplined production framework — ensuring reproducibility, traceability, and full documentation integrity at every stage.

01
Step 01

Specification Review

We assess your peptide compound, target dosage, and product requirements against our manufacturing capabilities.

02
Step 02

Production Planning

Process parameters are validated and batch records structured prior to any manufacturing run.

03
Step 03

Controlled Synthesis

Peptide synthesis and purification are executed under validated protocols with full traceability.

04
Step 04

QA/QC & Release

Analytical testing, QA review, and batch release documentation are completed before final handoff.

OEM Capabilities

Our manufacturing infrastructure covers every phase from synthesis through finished packaging — coordinated within a single production framework.

Custom Peptide Synthesis

Executed under validated synthesis processes with documented purity and yield parameters.

Controlled Purification Protocols

HPLC-based purification to defined specification grades with full traceability.

Lyophilized & Liquid Sterile Formats

Parenteral-grade dosage form manufacturing in both lyophilized powder and sterile liquid configurations.

Dosage-Form Manufacturing

Fill-finish operations aligned to your defined dosage parameters and container specifications.

Analytical Testing Coordination

Structured QA/QC oversight including identity, purity, potency, and sterility testing.

Packaging & Batch Release

Labeling execution and complete batch release documentation for regulatory compliance.

We operate under disciplined manufacturing controls to ensure reproducibility, traceability, and regulatory documentation integrity across every production run.

Start an OEM Inquiry

Ready to Begin Your OEM Project?

Submit your product specifications and our team will assess alignment with our manufacturing capabilities.

SUBMIT INQUIRYVIEW ODM OPTION

Start Your

Manufacturing Project

17654 Newhope St STE D, Fountain Valley, CA 92780, USA

28-10, Tojeong-ro, Mapo-gu, Seoul, Republic of Korea 04085

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+82 10 6399 4897

info@thetruepharma.com

The True Pharmaceutical|