OEM Private Label Services

One-stop OEM peptide solutions for brands, distributors, and research institutions — from formulation to delivery, fully managed by a dedicated project team.

Custom Formulation Sequence design, modification optimization, and formulation development tailored to your target product profile, with sample confirmation before production.

Private Label Packaging Your brand on the label, our quality inside the vial. Multi-spec filling (1mg to 100mg+ per vial), custom label and box design, and tamper-evident finishing.

Full Registration Dossier Complete regulatory support documentation — quality standards, testing protocols, and stability data — prepared to accelerate your market entry.

Global Logistics Lyophilized products packed with cold-chain protection and shipped through international express networks with tracking from our dock to yours.

Rigorous Quality Control Every OEM batch runs the full analytical panel — HPLC purity, MS identity, peptide content, water content, and endotoxin — before release.

Dedicated Account Service A single project manager tracks your OEM order from start to finish, providing technical consultation during development and after-sales support.

OEM Collaboration Process

A five-step workflow that takes your project from first contact to delivered, labeled product.

Requirement discussion
Share your target peptide, quantity, purity, and packaging needs. Our specialists review sequence feasibility and respond with a technical proposal.
Sample confirmation
We produce a pilot batch with your chosen formulation and packaging plan; you approve the sample before commercial production begins.
Terms and kick-off
Confirm technical and commercial terms, sign the supply agreement, and officially start the project with a dedicated project manager.
Production and QC
Synthesis, purification, lyophilization, filling, and full analytical QC run under batch-record control with QA-reviewed release.
Delivery and support
Cold-chain international shipping with tracking, complete COA documentation, and after-sales technical support for your customers.

Ready to start your OEM project?

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Contact OEM Specialists

Quality Agreement & Responsibility Split

For every OEM program, responsibilities are defined before production starts, not discovered after delivery.

Item	Shandong Shengyuan	Brand / Buyer
Specification & acceptance criteria	Drafts against analytical capabilities; confirms feasibility	Approves final specification in writing
Manufacturing & batch records	Executes; retains complete batch records	Right to audit summary records on request
QC testing & release	Runs full analytical panel; QA-gated release	May commission independent third-party testing
Label & packaging compliance	Manufactures to approved artwork	Owns label content and destination-country compliance
Change control & deviations	Notifies and documents any change or deviation	Approves material changes before implementation

Batch Definitions

Development batch — small-scale synthesis to confirm sequence, purity profile, and process feasibility before commitment.
Pilot batch — process-representative scale with the final specification and packaging configuration; shipped for buyer approval.
Commercial batch — full production against the approved specification, batch record, and quality agreement.

The process steps below describe a typical program. Projects are quoted individually; lead times and scope are confirmed in the quotation, not from marketing text.