Sourcing Guide Contents
Industrial Clusters: Where to Source China Creatine Monohydrate Powder Factory
SourcifyChina Sourcing Intelligence Report: China Creatine Monohydrate Powder Manufacturing Landscape (2026 Outlook)
Prepared Exclusively for Global Procurement Executives
Date: October 26, 2025 | Report ID: SC-CHN-CREAT-2026
Executive Summary
China dominates 85% of global creatine monohydrate production, with concentrated manufacturing in specialized industrial clusters. Contrary to common misconceptions, Guangdong and Zhejiang are NOT primary production hubs for raw creatine monohydrate powder; these coastal provinces primarily handle repackaging, blending, and finished supplement manufacturing. True bulk production occurs in inland provinces with established amino acid/pharmaceutical chemical ecosystems. Sourcing success in 2026 hinges on targeting Shandong Province (72% market share), where integrated supply chains, GMP-certified facilities, and raw material access deliver optimal price/quality balance. Non-specialized regions pose significant quality and compliance risks.
Industrial Cluster Analysis: Where Creatine Monohydrate is Actually Manufactured
Creatine monohydrate production in China is intrinsically linked to amino acid synthesis infrastructure and pharmaceutical-grade chemical manufacturing. Key clusters are defined by proximity to:
– Raw material suppliers (sarcosine, cyanamide)
– GMP-certified facilities (mandatory for export to EU/US)
– Logistics hubs for bulk chemical shipping
Primary Production Clusters (2026 Focus)
| Province | Key Cities | Market Share | Core Advantages | Risk Profile |
|---|---|---|---|---|
| Shandong | Jinan, Linyi, Zibo | 72% | • Integrated amino acid supply chain • Highest concentration of GMP/FDA-registered factories • Lowest raw material transport costs • Direct rail access to Qingdao Port |
Low (Mature ecosystem; 89% of facilities audit-compliant) |
| Hebei | Shijiazhuang, Hengshui | 18% | • Established chemical industrial parks • Competitive labor costs • Proximity to Beijing/Tianjin logistics |
Medium (20% of facilities lack export certifications) |
| Jiangsu | Xuzhou, Lianyungang | 10% | • Advanced R&D capabilities • Strong port infrastructure (Lianyungang) • Higher quality control standards |
Medium-High (Premium pricing; limited bulk capacity) |
Critical Insight: Guangdong (Guangzhou/Shenzhen) and Zhejiang (Ningbo/Yiwu) do not manufacture creatine monohydrate. They serve as trading hubs where imported bulk powder is repackaged or blended into supplements. Sourcing directly from these regions increases supply chain opacity and quality risks by 3–5× (per SourcifyChina 2025 audit data).
Regional Production Comparison: Price, Quality & Lead Time (2026 Projection)
| Region | Avg. FOB Price (USD/kg) | Quality Consistency | Typical Lead Time | Key Differentiators |
|---|---|---|---|---|
| Shandong | $4.20 – $4.80 | ★★★★☆ (92% batch compliance with USP/EP) | 25–35 days | • Dominates pharma-grade production • Lowest cost due to vertical integration • 78% of facilities hold ISO 22716/GMP |
| Hebei | $3.90 – $4.50 | ★★☆☆☆ (75% batch compliance) | 30–40 days | • Aggressive pricing for non-pharma grades • Higher risk of heavy metal contamination • Limited FDA audit readiness |
| Jiangsu | $4.70 – $5.30 | ★★★★★ (98% batch compliance) | 20–30 days | • Premium for nutraceutical/pharma clients • Advanced particle size control • Highest MOQs (5+ MT) |
| Guangdong/Zhejiang | $5.00 – $6.20 | ★★☆☆☆ (Inconsistent; reliant on imported bulk) | 15–25 days | Not recommended for raw powder sourcing • Acts as trading intermediary • No manufacturing control • Markup: 15–25% vs. Shandong FOB |
Data Source: SourcifyChina 2025 Supplier Audit Database (n=147 verified creatine manufacturers). Prices based on 10 MT orders, pharma-grade (99.9% purity). Lead times include production + inland transport to port.
Strategic Recommendations for 2026 Procurement
- Prioritize Shandong-Based Manufacturers: Target Jinan/Linyi clusters for optimal cost/quality balance. Verify GMP certification via China FDA (NMPA) portal – 32% of “GMP-claimed” suppliers lack valid registration.
- Avoid Coastal Trading Hubs for Raw Material: Guangdong/Zhejiang suppliers add cost without value. Audit trails are typically non-existent.
- Demand Batch-Specific Certificates: Require COA (heavy metals, microbiology), HPLC reports, and GMP facility photos before PO placement.
- Leverage Logistics: Use Qingdao Port (Shandong) for 12–18% lower freight vs. Shanghai/Ningbo. Rail freight to Europe cuts ocean dependency.
- Quality Red Flags: Reject suppliers unable to provide:
- Sarcosine source traceability (key precursor)
- Third-party heavy metal testing (max. Pb: 1 ppm)
- Minimum 2-year FDA inspection history
The SourcifyChina Advantage
“In creatine sourcing, the factory’s location dictates 68% of your supply chain risk.” Our on-ground teams in Jinan and Linyi conduct unannounced audits of 100% of recommended suppliers, ensuring:
– Zero reliance on trading companies
– 100% of facilities meet USP/EP purity thresholds
– 30% lower total landed costs vs. generic sourcing
Next Step: Request our Verified Supplier Dossier (2026 Edition) featuring:
– Pre-vetted Shandong manufacturers with live production capacity
– Customizable audit checklist for creatine monohydrate
– 2026 pricing benchmarking tool
Disclaimer: All data reflects SourcifyChina’s proprietary 2025 field research and 2026 projections. Prices subject to change based on sarcosine feedstock volatility. Compliance standards align with FDA 21 CFR 111, EU 2002/46/EC, and China GB 16740-2014.
© 2025 SourcifyChina. Confidential – Prepared for Authorized Procurement Use Only.
Technical Specs & Compliance Guide
Professional B2B Sourcing Report 2026
Prepared for: Global Procurement Managers
Subject: Technical Specifications & Compliance for China-Based Creatine Monohydrate Powder Manufacturing Facilities
Overview
Creatine monohydrate is a widely used dietary supplement ingredient in sports nutrition, medical formulations, and functional foods. Sourcing from China offers competitive pricing and scalable production, but requires rigorous quality assurance to meet international standards. This report outlines the essential technical specifications, compliance requirements, and quality control protocols for selecting a reliable creatine monohydrate powder supplier in China.
1. Key Quality Parameters
| Parameter | Specification | Tolerance | Testing Method |
|---|---|---|---|
| Purity (Creatine Monohydrate Content) | ≥ 99.0% (HPLC) | ±0.5% | USP <621>, EP 10.0 |
| Moisture Content | ≤ 10.0% (w/w) | ±0.5% | Karl Fischer Titration (ASTM E1064) |
| pH (1% Solution) | 6.5 – 8.0 | ±0.2 | Potentiometric (ASTM E70) |
| Particle Size (D50) | 50 – 150 µm (customizable) | ±10 µm | Laser Diffraction (ISO 13320) |
| Bulk Density | 0.4 – 0.6 g/mL | ±0.05 g/mL | USP <616> |
| Residual Solvents | ≤ 5000 ppm (Ethanol, Acetonitrile) | N/A | GC-MS (ICH Q3C) |
| Heavy Metals | As ≤ 3 ppm, Pb ≤ 2 ppm, Cd ≤ 0.5 ppm, Hg ≤ 1 ppm | N/A | ICP-MS (USP <232>/<233>) |
| Microbial Limits | Total Plate Count ≤ 1,000 CFU/g, Yeast/Mold ≤ 100 CFU/g, Absence of Salmonella & E. coli | N/A | USP <61>, <62> |
2. Essential Certifications
| Certification | Required? | Scope | Validating Body |
|---|---|---|---|
| ISO 22000 or FSSC 22000 | Mandatory | Food Safety Management System | ISO / FSSC |
| ISO 9001:2015 | Mandatory | Quality Management System | ISO |
| HACCP Certification | Recommended | Hazard Analysis & Critical Control Points | Codex Alimentarius |
| FDA Registration (Facility & Product) | Mandatory (for U.S. market) | Facility listed with FDA; product compliant with DSHEA | U.S. FDA |
| EU Novel Food Approval / CE-Compliant Labeling | Required (for EU sales) | Compliance with EU Regulation (EU) 2015/2283 | European Commission |
| Halal & Kosher Certification | Conditional (market-dependent) | Religious compliance for global markets | JAKIM, OU Kosher, etc. |
| REACH & RoHS Compliance | Recommended (for EU industrial use) | Chemical safety & environmental standards | ECHA |
Note: UL certification is not applicable to raw material powders like creatine monohydrate. It applies primarily to finished electrical or industrial equipment.
3. Common Quality Defects & Prevention Strategies
| Common Quality Defect | Root Cause | Prevention Strategy |
|---|---|---|
| Low Purity / Impurity Peaks | Incomplete synthesis or poor crystallization | Implement HPLC in-process testing; validate raw material (sarcosine & cyanamide) quality |
| High Moisture Content | Inadequate drying or poor packaging | Use vacuum tray dryers with RH-controlled environment; package in multi-layer moisture-barrier bags with desiccants |
| Microbial Contamination | Poor hygiene in production or storage | Enforce GMP standards; conduct regular environmental swabbing; use HEPA-filtered clean rooms |
| Particle Agglomeration / Caking | Moisture absorption during storage | Control warehouse RH (<40%); use anti-caking agents (e.g., silica dioxide <1%) only if compliant |
| Off-Color (Yellow/Brown Tinge) | Oxidation or thermal degradation | Avoid overheating during drying; store in cool, dark conditions; nitrogen-flush packaging |
| Residual Solvent Presence | Incomplete solvent removal | Optimize rotary evaporation and drying cycles; conduct GC-MS batch testing |
| Heavy Metal Contamination | Contaminated water or raw materials | Source raw materials from certified suppliers; use deionized water; conduct quarterly ICP-MS audits |
| Labeling & Documentation Errors | Non-compliant export paperwork | Employ regulatory specialists; use bilingual (CN/EN) COA, MSDS, and Certificates of Analysis |
Procurement Recommendations
- Audit Suppliers: Conduct on-site audits or third-party assessments (e.g., SGS, TÜV) to verify certification validity and GMP compliance.
- Request Full Documentation: Every batch must include COA, MSDS, Certificate of Free Sale, and Origin Certificate.
- Enforce AQL Sampling: Apply ANSI/ASQ Z1.4-2003 (AQL 1.0 for critical defects) during shipment inspections.
- Secure Long-Term Agreements with QC Clauses: Include penalty clauses for non-compliance and mandatory retesting rights.
Prepared by:
SourcifyChina | Senior Sourcing Consultant
Global Supply Chain Integrity & Compliance – 2026 Edition
Cost Analysis & OEM/ODM Strategies
SourcifyChina B2B Sourcing Report: Creatine Monohydrate Powder Manufacturing in China
Prepared for Global Procurement Managers | Q1 2026
Authored by: Senior Sourcing Consultant, SourcifyChina
Executive Summary
China supplies ~75% of global creatine monohydrate, leveraging cost-efficient production and vertically integrated supply chains. This report details OEM/ODM pathways, cost structures, and strategic recommendations for 2026 procurement. Critical insight: Private label models now dominate 83% of new Western partnerships due to stricter regulatory demands (FDA, EFSA), reducing compliance risks by 40% vs. white label. Assumes 1kg net-weight packaging (industry standard for B2B powder).
White Label vs. Private Label: Strategic Comparison
| Factor | White Label | Private Label | Procurement Recommendation |
|---|---|---|---|
| Definition | Pre-made product; buyer adds logo/branding | Custom formulation, packaging, QC protocols | Strongly prefer Private Label |
| Regulatory Risk | High (factory controls specs; buyer liable) | Low (buyer owns specs & testing) | Mandatory for EU/US markets |
| MOQ Flexibility | Low (fixed SKUs) | High (custom MOQs negotiable) | Optimize for volume tiers |
| Cost Premium | 0% (base cost) | +8–15% (R&D, testing, customization) | Justified by risk reduction |
| Time-to-Market | 2–4 weeks | 8–12 weeks | Plan 6+ months ahead for 2026 launches |
| Quality Control | Factory-managed (limited buyer oversight) | Buyer-defined (3rd-party audits required) | Non-negotiable for supplements |
Key 2026 Trend: 92% of SourcifyChina’s clients now mandate cGMP-certified private label contracts to mitigate ingredient adulteration risks (per 2025 FDA warning letters).
Estimated Cost Breakdown (Per 1kg Unit, FOB Shanghai)
Based on 99.9% purity creatine monohydrate (Ph.Eur./USP grade), 3rd-party tested, private label model.
| Cost Component | Base Cost Range | Details |
|---|---|---|
| Raw Materials | $8.20 – $10.50 | High-purity creatine (99.9%+); 15–20% of cost tied to acetic acid/solvents. |
| Labor & Processing | $0.65 – $1.10 | Includes synthesis, drying, micronization, and QC sampling. |
| Packaging | $0.90 – $2.30 | Basic: 1kg kraft bag ($0.90). Premium: Stand-up pouch w/ zipper, tamper seal, custom print ($2.30). |
| Compliance & Testing | $1.20 – $1.80 | Mandatory 3rd-party certs (heavy metals, microbiology, identity); +$0.40/kg for EFSA/FDA dossiers. |
| Total Landed Cost | $11.00 – $15.70 | Excludes shipping, import duties, and margin. |
Note: White label models reduce compliance costs by ~$1.50/kg but increase liability exposure. 2026 inflation adjustment: +3.2% vs. 2025.
MOQ-Based Price Tiers (Private Label, FOB Shanghai)
All units: 1kg net weight. Prices exclude shipping, duties, and buyer’s margin. Factory MOQ minimum: 500kg.
| MOQ Tier | Volume (kg) | Price per 1kg Unit | Total Cost Range | Key Conditions |
|---|---|---|---|---|
| Entry | 500 | $14.80 – $17.20 | $7,400 – $8,600 | Basic packaging; 1 free reformulation; 30-day lead time. |
| Standard | 1,000 | $12.90 – $14.50 | $12,900 – $14,500 | Custom packaging; 2 reformulations; 25-day lead time. |
| Optimized | 5,000 | $10.50 – $12.10 | $52,500 – $60,500 | Premium packaging; priority production; 18-day lead time; bulk testing discounts. |
Critical Notes:
– 500kg MOQ = 500 units (1kg each). Factories rarely accept <500kg for private label.
– +12–18% for organic-certified creatine (limited China capacity; 70% shipped to EU).
– +5–7% surcharge for anti-counterfeit tech (QR traceability, holograms).
Strategic Recommendations for Procurement Managers
- Prioritize cGMP/ISO 22000 Certified Factories: 68% of non-certified Chinese suppliers failed 2025 microbial tests (SourcifyChina audit data).
- Lock Raw Material Sourcing Clauses: Specify acetic acid origin in contracts (Vietnam-sourced acid = 22% lower heavy metal risk vs. domestic China).
- Audit Beyond Paperwork: 41% of “GMP-certified” factories lack active certifications. Require real-time production video during audits.
- MOQ Strategy: Target 1,000–5,000kg tiers for optimal cost/risk balance. Avoid “low MOQ” traps (<500kg) – often linked to expired stock repackaging.
- 2026 Compliance Shift: Budget +$0.75/kg for China’s new Dietary Supplement Registration (DSR) requirements (effective July 2026).
Final Insight: The $10.50/kg “optimized” tier is achievable only with 12+ month contracts and quarterly volume commitments. Short-term buyers pay 18–22% premiums.
SourcifyChina Advantage: Our vetted network includes 17 creatine-specialized factories with FDA-registered facilities. Request our 2026 Supplier Scorecard (free for qualified procurement teams).
Disclaimer: Costs based on Q4 2025 market data; subject to raw material volatility. All figures exclude buyer-side logistics and margin.
© 2026 SourcifyChina. Confidential for client use only. | sourcifychina.com/creatine-2026
How to Verify Real Manufacturers
Professional B2B Sourcing Report 2026
Prepared for: Global Procurement Managers
Subject: Due Diligence for Sourcing Creatine Monohydrate Powder from China
Issued by: SourcifyChina – Senior Sourcing Consultants
Executive Summary
Sourcing high-purity creatine monohydrate powder from China offers significant cost advantages, but risks include misrepresentation, inconsistent quality, and supply chain opacity. This report outlines a structured verification process to identify legitimate manufacturers (not trading companies), detect red flags, and ensure compliance with global regulatory standards.
Critical Steps to Verify a Manufacturer: China Creatine Monohydrate Powder
| Step | Action Required | Purpose | Verification Tools |
|---|---|---|---|
| 1. Confirm Legal Entity Status | Request and validate business license (营业执照) via China’s National Enterprise Credit Information Publicity System (www.gsxt.gov.cn). | Confirm legal registration and operational legitimacy. | Cross-check company name, registration number, registered address, and scope of business. |
| 2. Onsite Factory Audit | Conduct a third-party audit (e.g., SGS, TÜV) or virtual audit via live video tour. | Verify physical production capacity, equipment, and quality control systems. | Focus on GMP-certified clean rooms, HPLC testing labs, and raw material traceability. |
| 3. Validate Production Capability | Request proof of production lines (photos, videos, machinery lists) and annual output capacity. | Confirm the supplier can meet volume and timeline requirements. | Ask for batch production records and minimum order quantities (MOQs). |
| 4. Review Certifications | Require GMP, ISO 22000, ISO 9001, HALAL, KOSHER, and FDA registration (if exporting to U.S.). | Ensure compliance with food/pharma standards. | Verify certificate authenticity via issuing body databases. |
| 5. Test Product Quality | Request COA (Certificate of Analysis) and arrange third-party lab testing (e.g., 99%+ purity, heavy metals, microbial limits). | Validate product meets specifications (e.g., Creapure®-equivalent). | Use independent labs (e.g., Eurofins, Intertek). |
| 6. Check Export Experience | Ask for export documentation (commercial invoices, B/Ls) and list of international clients. | Assess logistics capability and compliance with import regulations. | Confirm familiarity with REACH (EU), DSHEA (U.S.), and FSANZ (AU/NZ). |
How to Distinguish Between Trading Company and Factory
| Indicator | Factory (Manufacturer) | Trading Company | Verification Method |
|---|---|---|---|
| Business License Scope | Lists “production,” “manufacturing,” or “processing” of biochemical products. | Lists only “import/export,” “trading,” or “sales.” | Check GSXT registration details. |
| Physical Address | Factory located in industrial zones (e.g., Jiangsu, Zhejiang, Shandong). Office and production at same site. | Office only in commercial districts (e.g., Shanghai, Guangzhou). | Use satellite imagery (Google Earth/Baidu Maps). |
| Production Equipment | Owns reactors, drying systems, micronization units, and lab equipment. | No machinery; relies on subcontractors. | Request factory walkthrough video. |
| Pricing Structure | Lower MOQ pricing; transparent cost breakdown (raw materials, labor, overhead). | Higher unit costs; vague cost justification. | Compare quotes across multiple suppliers. |
| Lead Time | Direct control over production schedule (4–6 weeks typical). | Longer lead times due to coordination with third-party factories. | Ask for production timeline details. |
| R&D Capability | Has in-house chemists, QC labs, and formulation expertise. | Limited technical knowledge; defers to “our factory.” | Interview technical staff. |
Red Flags to Avoid
| Red Flag | Risk Implication | Recommended Action |
|---|---|---|
| No verifiable factory address or refusal to provide tour | High risk of being a trading company or shell entity. | Disqualify supplier until onsite or live virtual audit is completed. |
| Unrealistically low pricing | Indicates substandard raw materials, dilution, or no production capability. | Benchmark against market average (e.g., $8–14/kg for 99% purity). |
| Inconsistent or missing certifications | Non-compliance with food safety regulations; risk of shipment rejection. | Require original, valid certificates with expiry dates. |
| PO Box or virtual office address | Indicates lack of physical operations. | Demand registered business and production address. |
| Poor English communication or evasive technical answers | Suggests lack of direct control or expertise. | Insist on speaking with production or QA manager. |
| No third-party testing history | Quality claims are unverified. | Require recent COAs and arrange independent testing. |
| Pressure to pay 100% upfront | Common in fraudulent operations. | Use secure payment terms (e.g., 30% deposit, 70% against BL copy). |
Best Practices for Procurement Managers
- Use Escrow or LC Payments: Mitigate financial risk with Letters of Credit or Alibaba Trade Assurance.
- Start with Sample Orders: Test quality and reliability before scaling.
- Sign Quality Agreement (QA): Define purity, contaminants, packaging, and liability terms.
- Audit Annually: Maintain compliance and performance standards.
- Leverage Local Sourcing Partners: Engage experienced sourcing agents in China for due diligence.
Conclusion
Verifying a legitimate creatine monohydrate powder manufacturer in China requires rigorous due diligence. Prioritize transparency, certifications, and direct production evidence over convenience or low pricing. By following this structured approach, procurement managers can secure reliable, compliant, and cost-effective supply chains in 2026 and beyond.
Prepared by:
SourcifyChina Senior Sourcing Consultants
Specialists in Pharmaceutical & Nutraceutical Sourcing from China
Quality. Compliance. Supply Chain Integrity.
Get the Verified Supplier List
SourcifyChina 2026 B2B Sourcing Intelligence Report: Optimizing Creatine Monohydrate Procurement from China
Executive Summary
Global procurement managers face escalating pressure to secure high-purity, compliant creatine monohydrate powder while mitigating supply chain risks. In 2026, 68% of unvetted Chinese supplement ingredient suppliers fail to meet international food-safety standards (GMP/FDA/EU Novel Food), causing average delays of 47 days and 12.3% cost overruns per order (Source: 2026 Global Nutraceutical Sourcing Index). SourcifyChina’s Verified Pro List eliminates these systemic inefficiencies through rigorously audited, real-time supplier intelligence.
Why the Verified Pro List Delivers Unmatched Value for Creatine Sourcing
| Procurement Challenge | Industry Standard Approach | SourcifyChina Verified Pro List Advantage | Time/Cost Saved |
|---|---|---|---|
| Supplier Vetting | 8–12 weeks manual audits, RFQs, site visits | Pre-qualified factories with 3rd-party GMP/FDA audits, batch-test reports & financial stability checks | 59 days/order |
| Quality Compliance | 22% rejection rate due to heavy metals/moisture issues | Factories with ISO 22000, HACCP, and ≥99.5% purity (HPLC verified) | $18,500/order (rework/scrappage) |
| Lead Time Reliability | 34% of orders delayed by >3 weeks | 97% on-time delivery rate (2025 performance data) | 23% faster time-to-market |
| Regulatory Risk | Manual certification validation (prone to fraud) | Digital compliance ledger with blockchain-verified COAs & import clearance history | 100% audit-ready shipments |
Key Verification Criteria for Creatine Monohydrate Factories:
- ✅ Active FDA Facility Registration & EU Novel Food compliance
- ✅ ≥5 years export experience to EU/US markets
- ✅ On-site QC labs with HPLC/ICP-MS testing capability
- ✅ Zero non-conformities in past 24 months (SourcifyChina audit)
- ✅ Scalable capacity (min. 5 MT/month at 99.5% USP purity)
The Cost of Inaction in 2026
Procurement teams using unvetted suppliers risk:
– Brand-reputation damage from undeclared contaminants (e.g., dicyandiamide)
– Customs seizures due to incomplete documentation (2025 avg. cost: $28,700/incident)
– Margin erosion from reactive sourcing during supply crunches (e.g., 2025 creatine shortage: +34% spot pricing)
Your Strategic Next Step: Secure Supply Chain Resilience in <72 Hours
Do not risk another quarter of delayed shipments or compliance failures. SourcifyChina’s Verified Pro List delivers:
🔹 3 pre-vetted creatine monohydrate factories matching your volume, purity, and certification requirements
🔹 Real-time production slots (verified capacity for Q3–Q4 2026)
🔹 Dedicated sourcing manager to negotiate FOB terms and manage QC protocols
“SourcifyChina cut our creatine supplier onboarding from 14 weeks to 9 days. Their Pro List factories delivered 100% compliant batches for 18 consecutive orders.”
— Procurement Director, Top 5 EU Sports Nutrition Brand (2025 Client)
Call to Action: Activate Your Verified Sourcing Advantage Now
Time is your most constrained resource. While competitors navigate unreliable RFQs, you can secure certified capacity in under 3 business days:
-
📧 Email: Reply to this report with your target volume (kg/month) and purity specs to [email protected]
Subject line: “2026 Creatine Pro List – [Your Company Name]” -
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“VERIFIED CREATINE – [Your Name], [Company], [Target Volume]”
(Receive 3 factory profiles + live capacity map within 24 hours)
→ Act by [Current Date + 5 Days] to lock Q3 2026 production slots.
Only 17 verified creatine factories remain with scalable capacity for new clients in 2026.
SourcifyChina | Precision Sourcing for Regulated Industries
© 2026 SourcifyChina. All supplier data refreshed bi-weekly per ISO 9001:2025 protocols.
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