OEM Manufacturing Facility
OEM & Contract Manufacturing

Your Brand.
Our Expertise.
End-to-End.

From custom peptide synthesis to finished, shelf-ready products — AODT Peptide is your GMP-certified manufacturing partner. We handle everything so you can focus on growing your brand.

500+
OEM Clients Served
50+
Countries Exported
GMP
Certified Facility
NDA
IP & Confidentiality
1mg–kg
Any Batch Scale
24h
Quote Response Time
Our Services

Complete OEM & CMO
Service Portfolio

Whether you need a single custom peptide or a fully finished branded product line, we have the capabilities to deliver at every stage of your supply chain.

OEM Custom Synthesis
Any Sequence. Any Scale. Your Brand.

OEM Custom Synthesis

We manufacture peptides to your exact specifications — sequence, purity, modifications, and scale. From 1 mg research quantities to multi-kilogram commercial batches, all under your brand with full white-label packaging and QC documentation.

Any amino acid sequence & chemical modification
1 mg to multi-kg batch sizes
White-label vials, kits, and packaging
Full CoA, HPLC, MS documentation
≥98% purity guaranteed by HPLC
Standard 2–4 weeks, express available
Private Label & Branding
Launch Your Own Peptide Product Line

Private Label & Branding

No manufacturing facility? No problem. We handle synthesis, QC testing, sterile filling, and custom labeling — you focus on sales and marketing. Launch a professional peptide brand with as few as 100 units per SKU.

Custom label design & artwork support
Branded vials, boxes, and inserts
MOQ as low as 100 units per SKU
Retail-ready, clinic-ready packaging
Custom lot numbers & expiry dating
Drop-ship or bulk fulfillment options
Contract Manufacturing (CMO)
GMP-Compliant Production for Pharma & Biotech

Contract Manufacturing (CMO)

Full-service contract manufacturing for pharmaceutical, nutraceutical, and biotech companies. Our GMP-certified facility operates under ICH Q7 guidelines with complete batch records, regulatory dossier support, and third-party audit readiness.

GMP-certified, ICH Q7 compliant facility
Complete batch records & release testing
DMF / ASMF filing support for US & EU
In-house analytical & QC laboratory
Third-party audit & inspection ready
Scale-up from R&D to commercial production
Formulation & Fill Services
From Bulk API to Finished Dosage Form

Formulation & Fill Services

Beyond synthesis — we offer complete formulation development and fill-finish services. Lyophilization, sterile vial filling, multi-peptide combination stacks, and reconstitution kits. We deliver a finished, shelf-ready product.

Lyophilization (freeze-drying) services
Sterile vial & ampoule filling
Multi-peptide combination formulation
Reconstitution kit assembly
Stability testing & shelf-life studies
Oral, topical, and injectable formats
How It Works

From Inquiry to
Delivered Product

Our streamlined 6-step OEM process ensures transparency, quality, and on-time delivery — every single order.

STEP 01

Initial Inquiry

Reach out via WhatsApp, email, or our inquiry form. Share your requirements: peptide sequence, quantity, grade, packaging, and timeline. We respond within 24 hours.

Our business development team will review your requirements and assign a dedicated project manager to your account.

STEP 02

NDA & Quotation

We sign a mutual NDA to protect your IP and formulation details. Our technical team prepares a detailed quotation with pricing, timeline, and specifications.

All client information, sequences, and formulations are strictly confidential under our NDA agreement.

STEP 03

Feasibility & Pilot Batch

For new sequences or formulations, we conduct a feasibility study and produce a pilot batch (typically 10–50 mg). You receive a sample with full analytical data for approval.

Pilot batch includes HPLC chromatogram, mass spectrum, and CoA for your review and approval.

STEP 04

Production & QC

Upon sample approval, we proceed to full-scale production. Every batch undergoes rigorous in-process and final QC testing including HPLC purity, MS confirmation, and endotoxin testing.

GMP batches include complete batch records, in-process controls, and release testing by our QC laboratory.

STEP 05

Packaging & Labeling

Finished product is filled, lyophilized (if required), and packaged under your brand. Custom labels, inserts, and outer packaging are applied per your specifications.

We support custom vial sizes, label artwork, lot numbering, expiry dating, and multi-language labeling.

STEP 06

Shipping & Documentation

Products are shipped with full documentation: CoA, MSDS, packing list, and any required regulatory certificates. We handle export compliance for 50+ countries.

Cold-chain shipping available. We work with DHL, FedEx, and specialized pharma logistics providers.

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Technical Capabilities

What We Can
Do For You

Full technical specifications of our manufacturing, analytical, and regulatory capabilities — so you know exactly what you're getting.

Synthesis Capabilities

Peptide Length2–100+ amino acids
Batch Scale1 mg – multi-kg
Purity≥95%, ≥98%, ≥99%
ModificationsPEGylation, acetylation, amidation, cyclization, phosphorylation, fluorescent labeling
Synthesis MethodFmoc SPPS, Boc SPPS, solution-phase
Turnaround2–4 weeks standard; express available

Analytical & QC

Purity AnalysisReverse-phase HPLC (RP-HPLC)
Identity ConfirmationESI-MS, MALDI-TOF
Endotoxin TestingLAL assay (≤1 EU/mg)
Sterility TestingUSP <71> compliant
Moisture ContentKarl Fischer titration
Residual SolventsGC-MS analysis

Formulation & Fill

LyophilizationFreeze-drying for long-term stability
Sterile FillingVials, ampoules, pre-filled syringes
FormatsInjectable, topical, oral, nasal
Vial Sizes1 mL, 2 mL, 5 mL, 10 mL, 30 mL
Combination StacksMulti-peptide co-formulation
Reconstitution KitsPeptide + diluent + accessories

Regulatory Support

GMP StandardICH Q7, EU GMP Annex 11
DocumentationCoA, MSDS, batch records, stability data
DMF FilingUS FDA Drug Master File support
ASMFEuropean Active Substance Master File
Import/ExportCompliance for 50+ countries
AuditsThird-party audit & inspection ready

Certifications & Standards

Fully Certified. Audit-Ready. Globally Compliant.

ISO 9001:2015GMP CertifiedFDA RegisteredICH Q7EU GMP Annex 11ISO 14001

GMP Certified

ISO 9001 & ICH Q7

NDA Protected

Full IP confidentiality

50+ Countries

Global export capability

Dedicated PM

Your own project manager

24h Response

Fast quote turnaround

Scalable

mg to multi-kg batches

Trusted by 500+ AODT Peptide Clients

What our partners say about working with us

“AODT Peptide has been our exclusive OEM partner for 3 years. Their GMP documentation is impeccable, and the quality is consistent batch after batch. Our private label line has grown 300% since we switched to them.”

Dr. Marcus Webb

Dr. Marcus Webb

Founder, RegenMed Clinics

🇺🇸 United States

“The regulatory support team helped us navigate EU GMP requirements and ASMF filing. What would have taken us 6 months internally was done in 8 weeks. Exceptional service.”

Sophie Laurent

Sophie Laurent

Head of Procurement, BioPharm EU

🇫🇷 France

“We source all our catalog peptides and custom synthesis from AODT Peptide. The purity data is always above spec, and their technical team understands complex modifications that other suppliers can't handle.”

Kenji Tanaka

Kenji Tanaka

R&D Director, Peptide Sciences Japan

🇯🇵 Japan

FAQ

Common OEM
Questions Answered

Everything you need to know before starting your OEM partnership with AODT Peptide.

Our MOQ depends on the service type. For custom synthesis, we start from 1 mg for research-grade peptides. For private label products, the MOQ is typically 100 units per SKU. For GMP-grade contract manufacturing, MOQ starts at 1 gram. Contact us for a specific quote based on your requirements.

Timelines vary by complexity. Standard research-grade custom synthesis takes 2–4 weeks. GMP-grade production typically takes 6–12 weeks including QC release. Private label orders with existing formulations can be completed in 3–6 weeks. We offer express services for urgent requirements.

Absolutely. We sign a mutual Non-Disclosure Agreement (NDA) before any technical discussions begin. All client sequences, formulations, and business information are strictly confidential. We have never disclosed client information in our 10+ years of operation.

Yes. Our regulatory team has extensive experience with US FDA Drug Master File (DMF) submissions and European Active Substance Master File (ASMF) filings. We provide all necessary documentation including batch records, analytical data, stability studies, and manufacturing process descriptions.

Every order includes a Certificate of Analysis (CoA) with HPLC purity data, mass spectrum confirmation, appearance, and solubility. GMP orders additionally include batch manufacturing records, in-process control data, endotoxin testing results, sterility testing (if applicable), and residual solvent analysis.

Yes, this is one of our specialties. We can co-formulate multiple peptides into a single vial or kit, optimizing for compatibility, stability, and efficacy. We have developed hundreds of custom combination formulas for clients worldwide, including popular stacks like BPC-157+TB-500, CJC-1295+Ipamorelin, and custom weight loss combinations.

Yes. For private label clients, we offer direct drop-shipping to your end customers or bulk fulfillment to your warehouse. We work with DHL, FedEx, and specialized pharmaceutical logistics providers. Cold-chain shipping is available for temperature-sensitive products.

We currently export to 50+ countries across North America, Europe, Asia-Pacific, Middle East, and Latin America. Our team handles all export documentation, customs compliance, and import permits. Contact us to confirm availability for your specific country.

Still have questions? Our team is ready to help.

OEM facility
Start Your Partnership

Ready to Launch Your
Peptide Brand?

Join 500+ companies worldwide who trust AODT Peptide as their OEM manufacturing partner. Get a free consultation and quote within 24 hours.

24h quote response
NDA signed first
GMP certified
Ships to 50+ countries