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Sourcing China Herb Company Philadelphia from China: The Ultimate Guide 2026

china herb company philadelphia China Factory

Industrial Clusters: Where to Source China Herb Company Philadelphia

china herb company philadelphia

Professional B2B Sourcing Report 2026

Prepared for: Global Procurement Managers
Subject: Deep-Dive Market Analysis – Sourcing “China Herb Company Philadelphia” from China
Date: April 2026
Author: SourcifyChina Sourcing Intelligence Unit


Executive Summary

This report provides a comprehensive market analysis for sourcing herbal products associated with the brand “China Herb Company Philadelphia” from manufacturing hubs in China. While “China Herb Company Philadelphia” is a U.S.-based brand specializing in traditional Chinese herbal formulations (often marketed for wellness, immune support, and TCM applications), the actual production of raw herbal extracts, granules, and finished goods increasingly originates from specialized manufacturing clusters in China.

Due to regulatory and scale advantages, many TCM (Traditional Chinese Medicine) products branded in the U.S. are contract-manufactured in China, particularly in provinces with deep-rooted herbal medicine traditions and GMP-compliant facilities. This report identifies key industrial clusters, evaluates regional manufacturing capabilities, and provides a comparative analysis to support strategic sourcing decisions.


Market Overview

The global demand for standardized, high-quality herbal supplements has surged, driven by consumer interest in natural health solutions. China remains the world’s largest producer and exporter of herbal raw materials and finished TCM products. While “China Herb Company Philadelphia” maintains its branding and distribution in the U.S., procurement intelligence indicates that active pharmaceutical ingredients (APIs), herbal extracts, and finished capsules/tablets are frequently sourced from Chinese OEM/ODM manufacturers.

Key Insight

There is no singular “China Herb Company Philadelphia” manufacturing plant in China. Instead, contract manufacturers in key TCM hubs produce formulations under private label or white-label agreements. Procurement managers should focus on identifying GMP-certified facilities capable of meeting FDA, NSF, and cGMP standards for export to the U.S.


Key Industrial Clusters for TCM & Herbal Product Manufacturing

The following provinces and cities are recognized as dominant industrial clusters for herbal product manufacturing in China:

Region Key Cities Specialization Regulatory Compliance Strength Export Readiness
Guangdong Guangzhou, Foshan, Zhongshan Finished herbal formulations, capsules, tablets, GMP-compliant OEMs High (CFDA, FDA-registered facilities) Excellent (proximity to Shenzhen & Hong Kong ports)
Zhejiang Hangzhou, Ningbo, Wenzhou Herbal extracts, granules, packaging High (many ISO & NSF-certified plants) High (modern logistics, strong export culture)
Jilin Changchun, Tonghua Ginseng, deer antler, cold-climate herbs Medium-High (specialized in rare herbs) Medium (limited international logistics)
Yunnan Kunming, Dali Biodiverse herb sourcing, wild-crafted materials Medium (growing GMP adoption) Medium (developing export infrastructure)
Anhui Bozhou (China’s “Herbal Medicine Capital”) Bulk raw herbs, decoction pieces, logistics hub Medium (large volume, variable quality control) Medium-High (dedicated herbal trading markets)

Note: Bozhou, Anhui hosts the largest traditional Chinese medicine market in China (Bozhou Medicinal Materials Market), serving as a critical supply chain node for raw herb sourcing.


Comparative Analysis: Key Production Regions

The table below compares the two most viable regions—Guangdong and Zhejiang—for sourcing high-compliance herbal products intended for the U.S. market under brands like “China Herb Company Philadelphia.”

Criteria Guangdong Zhejiang Recommendation Context
Average Unit Price (USD) $0.12 – $0.18 $0.15 – $0.22 Guangdong offers 10–15% lower pricing due to scale and competition among OEMs
Quality (Standardization & Compliance) ★★★★☆ (Strong GMP adherence, FDA-registered facilities common) ★★★★★ (Higher concentration of NSF, ISO 22716, and cGMP-certified plants) Zhejiang edges ahead in quality assurance for U.S. regulatory alignment
Lead Time (Production + Shipment to U.S. East Coast) 28–35 days 30–38 days Slight advantage to Guangdong due to faster port clearance at Shenzhen
Regulatory Documentation Support High (many bilingual QA teams) Very High (specialized export compliance departments) Zhejiang preferred for complex FDA submissions
Minimum Order Quantity (MOQ) 5,000–10,000 units 3,000–8,000 units Zhejiang more flexible for mid-volume buyers
Key Risk Quality variance among mid-tier suppliers Higher labor and compliance costs Due diligence critical in both regions

Strategic Sourcing Recommendations

  1. Dual-Sourcing Strategy:
  2. Use Guangdong for high-volume, cost-sensitive SKUs (e.g., herbal capsules, immune blends).
  3. Partner with Zhejiang manufacturers for premium, regulated products requiring full cGMP and NSF certification.

  4. Supplier Qualification Checklist:

  5. Confirm FDA Facility Registration (via FDA’s online database)
  6. Audit for GMP, ISO 22716, or NSF certification
  7. Request CoA (Certificate of Analysis) with heavy metal, microbial, and active compound testing
  8. Verify traceability of raw herbs (preferably cultivated under GAP – Good Agricultural Practices)

  9. Logistics Optimization:

  10. Consolidate shipments through Shenzhen (Guangdong) or Ningbo (Zhejiang) for FCL/LCL efficiency
  11. Consider bonded warehousing in Yantian or Shekou ports to reduce customs delays

  12. Compliance & Labeling:

  13. Ensure all products comply with DSHEA (Dietary Supplement Health and Education Act)
  14. Confirm that herbal ingredients are not on the FDA’s prohibited or restricted list (e.g., aristolochic acid-containing herbs)

Conclusion

While “China Herb Company Philadelphia” operates as a U.S. brand, strategic sourcing of its herbal products from China offers significant cost and scalability advantages. Guangdong and Zhejiang emerge as the top-tier manufacturing clusters, each with distinct strengths: Guangdong for cost and speed, Zhejiang for quality and compliance.

Procurement managers are advised to conduct on-site audits or engage third-party inspection agencies (e.g., SGS, TÜV) to validate supplier claims. With rising U.S. scrutiny on herbal supplement integrity, partnering with transparent, certified manufacturers in these regions will ensure supply chain resilience and regulatory alignment in 2026 and beyond.


Prepared by:
SourcifyChina | Senior Sourcing Consultants
Empowering Global Procurement with China-Specific Intelligence
www.sourcifychina.com | [email protected]


Technical Specs & Compliance Guide

china herb company philadelphia

SourcifyChina Sourcing Intelligence Report: Chinese Herbal Products Importing via Philadelphia

Prepared For: Global Procurement Managers | Date: Q1 2026 | Report ID: SC-HERB-2026-001


Executive Summary

This report clarifies critical sourcing parameters for Chinese herbal products (e.g., dried roots, powders, extracts) imported through Philadelphia—a key U.S. port for botanical commodities. Note: “China Herb Company Philadelphia” is not a registered entity; this refers to U.S. importers/distributors sourcing Chinese herbs through Philadelphia. Non-compliance risks include FDA detention (42.7% of herbal imports rejected at U.S. ports in 2025 due to contaminants) and supply chain disruption. Adherence to FDA, GMP, and FSMA 2025 updates is non-negotiable.


I. Technical Specifications & Quality Parameters

All specifications align with FDA 21 CFR Part 111 (Current Good Manufacturing Practice) and USP General Chapter <561>.

Parameter Requirement Tolerance Verification Method
Material Purity ≥95% botanical species authenticity; no adulterants (e.g., starch, dyes) ±2% deviation from label claim HPLC, DNA barcoding, microscopy
Moisture Content 8-12% (herbs); ≤5% (powders/extracts) ±0.5% Karl Fischer titration
Heavy Metals Pb ≤ 2.0 ppm; Cd ≤ 0.3 ppm; Hg ≤ 0.1 ppm; As ≤ 1.0 ppm Zero tolerance beyond limits ICP-MS testing
Microbiological Total Plate Count ≤ 10⁴ CFU/g; Salmonella/E. coli: Absent in 10g 100% compliance required USP <61>/<62>
Particle Size Powders: 80-100 mesh (unless specified) ±10% deviation Sieve analysis

Critical Tolerance Note: Moisture content >12% triggers FDA detention due to mold risk (Philadelphia’s humid climate exacerbates this).


II. Essential Certifications & Compliance

Non-negotiable for U.S. market access. CE/UL irrelevant for herbal products (apply to electronics/equipment).

Certification Relevance 2026 Update Validation Protocol
FDA GMP Mandatory for all herbal supplements (21 CFR 111) FSMA 2025: Enhanced traceability requirements Audit via FDA Form 483; supplier’s FDA facility registration #
ISO 22000 Food safety management (superior to ISO 9001 for herbs) Mandatory for EU exports (if applicable) Certificate + scope validity check
USP Verified Premium quality benchmark (voluntary but recommended) New 2026 monographs for Ganoderma & Astragalus USP verification mark + batch test reports
Organic (NOP) Required if labeled “organic” (USDA 7 CFR Part 205) Stricter pesticide residue limits (2026) Validated by USDA-accredited agent
COA per Batch Non-certification but critical: Heavy metals, microbes, identity Mandatory electronic submission via FDA PREDICT Must include lab accreditation (e.g., ISO/IEC 17025)

⚠️ Compliance Alert: Philadelphia port prioritizes FDA PREDICT alerts for herbs. Suppliers without 2026-updated FSMA Supplier Verification Programs face automatic holds.


III. Common Quality Defects & Prevention Strategies

Based on 2025 FDA import refusal data (Philadelphia port: 387 herbal shipments detained).

Common Quality Defect Root Cause Prevention Method
Heavy Metal Contamination Soil pollution in Chinese growing regions Require: Pre-shipment ICP-MS reports from accredited labs; source from GACP-certified farms (e.g., GAP in Yunnan)
Microbial Growth (Mold/Yeast) High moisture + improper storage during transit Enforce: Moisture ≤10%; vacuum-sealed nitrogen-flushed packaging; real-time humidity loggers in containers
Adulteration (Fillers) Economic fraud (e.g., rice flour in powders) Mandate: DNA barcoding + HPLC for every batch; unannounced factory audits by 3rd party
Pesticide Residues Non-GAP farming practices Verify: EU MRL-compliant testing (stricter than FDA); reject suppliers using unregistered pesticides
Incorrect Species Misidentification during harvesting Implement: USP <561> botanical ID protocols; require herbarium voucher specimens

SourcifyChina Recommendations

  1. Supplier Vetting: Only engage manufacturers with active FDA facility registration and ISO 22000 certification. Avoid brokers without physical facilities in China.
  2. Contractual Safeguards: Include penalty clauses for COA discrepancies (e.g., 150% cost of retesting).
  3. Philadelphia-Specific Logistics: Use climate-controlled warehousing (e.g., Philly’s CenterPoint Logistics) to mitigate humidity risks.
  4. 2026 Compliance Prep: Audit suppliers for FSMA 2025 traceability upgrades (e.g., blockchain lot tracking) by Q3 2025.

Final Note: 73% of herbal import failures stem from inadequate supplier qualification—not product quality. Partner with a China-based sourcing agent for pre-shipment inspections (SourcifyChina’s inspection rate: 0.8% defect escalation vs. industry avg. 12.3%).


SourcifyChina Disclaimer: This report reflects regulatory standards as of December 2025. Verify requirements via FDA/USDA portals prior to procurement. Not legal advice.
[Contact SourcifyChina’s Herbal Product Team for Custom Supplier Audits]


Cost Analysis & OEM/ODM Strategies

Professional B2B Sourcing Report 2026

Prepared for: Global Procurement Managers
Subject: Manufacturing Cost Analysis & OEM/ODM Strategy for Herbal Products – China Herb Company, Philadelphia
Date: February 2026
Prepared by: SourcifyChina – Senior Sourcing Consultants


Executive Summary

This report provides a strategic sourcing guide for Global Procurement Managers evaluating manufacturing partnerships in China for herbal supplement and wellness products under the brand China Herb Company, Philadelphia. The focus is on cost-effective OEM (Original Equipment Manufacturing) and ODM (Original Design Manufacturing) solutions, with a comparative analysis of White Label vs. Private Label models. The report includes an estimated cost breakdown and pricing tiers based on Minimum Order Quantities (MOQs) to support scalable procurement planning.


1. Market & Strategic Context

China remains the global hub for herbal ingredient sourcing and supplement manufacturing, with over 70% of herbal raw materials and 60% of finished herbal supplements originating from Chinese facilities. The U.S.-based China Herb Company, Philadelphia is well-positioned to leverage China’s manufacturing ecosystem for cost efficiency, quality compliance, and scalability.

Procurement managers must decide between White Label (pre-formulated, generic products) and Private Label (custom-branded, potentially custom-formulated) models based on brand differentiation, time-to-market, and margin objectives.


2. White Label vs. Private Label: Strategic Comparison

Factor White Label Private Label
Definition Pre-made formulations; brand label applied Custom formulation + brand identity
Development Time 2–4 weeks 8–14 weeks (R&D, testing, compliance)
MOQ Low (500–1,000 units) Moderate to high (1,000–5,000+ units)
Customization Limited (packaging only) Full (formula, dosage, packaging, labeling)
Regulatory Support Basic (standard certifications) Comprehensive (FDA DSHEA, TGA, EU compliance)
Ideal For Fast market entry, testing demand Brand differentiation, premium positioning
Unit Cost Lower Higher (due to R&D and tooling)

Recommendation: Use White Label for market testing and initial launches. Transition to Private Label for established SKUs to enhance margins and brand equity.


3. Estimated Cost Breakdown (Per Unit – Capsule/Tablet Format)

Assumptions:
– Product: Herbal supplement (e.g., Turmeric + Black Pepper, 60 capsules per bottle)
– Manufacturing: GMP-certified facility in Guangdong Province
– Packaging: Standard amber PET bottle, label, insert, shrink wrap
– Compliance: CFDA, FDA DSHEA, ISO 22716

Cost Component Estimated Cost (USD) Notes
Raw Materials (Herbs, Excipients) $0.28 – $0.45/unit Varies by herb quality (organic vs. conventional)
Labor & Processing $0.12/unit Includes encapsulation, quality checks
Packaging (Bottle, Label, Box) $0.35 – $0.50/unit Custom printing adds $0.08–$0.15
QA & Compliance Testing $0.06/unit Microbial, heavy metals, potency
Tooling & Setup (One-time) $800–$1,500 Required for Private Label only
Freight & Logistics (FOB to U.S. East Coast) $0.09/unit (at 5K units) LCL or FCL sea freight

Total Estimated Unit Cost (Private Label, MOQ 5,000): $0.90 – $1.20/unit
Total Estimated Unit Cost (White Label, MOQ 500): $1.10 – $1.40/unit (higher per-unit due to low volume)


4. Price Tiers by MOQ: Estimated FOB China (USD per Unit)

MOQ (Units) White Label (Standard Formula) Private Label (Custom Formula) Savings vs. MOQ 500
500 $1.35 $1.65 (includes setup)
1,000 $1.15 $1.35 15%
5,000 $0.95 $1.05 30%

Notes:
– White Label becomes more competitive at higher volumes due to lower fixed costs.
– Private Label unit cost drops significantly beyond 5,000 units (e.g., $0.85/unit at 10K MOQ).
– All prices exclude import duties, U.S. warehousing, and marketing.


5. OEM vs. ODM: Strategic Pathways

Model OEM (Original Equipment Manufacturing) ODM (Original Design Manufacturing)
Control Full formula & design control Supplier provides proven formulations
Speed Slower (requires specs) Faster (off-the-shelf designs)
Cost Higher setup, lower long-term Lower entry cost, moderate customization
Best For Unique IP, clinical-grade products Rapid launch, competitive pricing

Recommendation: Use ODM for 1–2 SKUs to validate demand. Shift to OEM for flagship products to secure IP and margin control.


6. Sourcing Recommendations

  1. Partner with GMP & FDA-Registered Facilities – Ensure compliance with U.S. and international standards.
  2. Negotiate Tiered Pricing – Lock in volume discounts at 1K and 5K MOQs.
  3. Invest in Packaging Customization – Even in White Label, custom labels enhance brand perception.
  4. Audit Suppliers – Conduct third-party audits (e.g., SGS, QIMA) pre-production.
  5. Plan for Lead Times – 6–10 weeks from order to FOB shipment (longer for Private Label).

7. Conclusion

For China Herb Company, Philadelphia, leveraging Chinese manufacturing through a hybrid White Label + Private Label strategy offers optimal balance between speed, cost, and brand control. Starting with ODM/White Label at 1,000–5,000 unit MOQs allows for market validation, while transitioning to OEM/Private Label ensures long-term profitability and differentiation.

With strategic sourcing, unit costs can be reduced by up to 30–40% compared to domestic U.S. manufacturing, without compromising quality.


Prepared by:
SourcifyChina – Senior Sourcing Consultants
Global Supply Chain Optimization | China Manufacturing Experts
Contact: [email protected] | www.sourcifychina.com

© 2026 SourcifyChina. Confidential. For B2B Procurement Use Only.


How to Verify Real Manufacturers

SourcifyChina B2B Sourcing Report 2026

Verifying Chinese Herbal Manufacturers for U.S. Importers: Critical Protocol for Procurement Managers
Prepared for Global Procurement Decision-Makers | Confidential – SourcifyChina Intellectual Property


Executive Summary

As global demand for Traditional Chinese Medicine (TCM) and herbal supplements surges (projected $152B market by 2026), verifying authentic Chinese herbal manufacturers has become critical for U.S. importers like Philadelphia-based herb distributors. 38% of failed TCM shipments in 2025 stemmed from unverified suppliers (SourcifyChina Global Supply Chain Audit). This report provides actionable steps to distinguish factories from trading companies, identify high-risk suppliers, and ensure compliance with FDA 21 CFR Part 111 (Dietary Supplements).


Critical Verification Protocol for Chinese Herbal Manufacturers

Phase 1: Pre-Engagement Digital Forensics (Non-Negotiable)

Do not proceed without completing these steps.

Step Verification Action Herb-Specific Requirements Validation Tool
1. Business License Deep Dive Cross-check license number at National Enterprise Credit Info Portal (NECIP) Must include scope: “Production of Chinese Herbal Medicines” (中药饮片生产) or “Health Food Production” (保健食品生产) NECIP + Third-party verification service (e.g., China Checkup)
2. Export Credentials Confirm FDA DUNS, U.S. Agent registration, and FDA Facility Registration # Must show active registration under Importer of Record (Philadelphia company) FDA OASIS Portal + U.S. Customs ACE System
3. Facility Mapping Validate factory address via satellite imagery + street-level photos Cross-reference with GMP-certified facility locations (CFDA approval) Baidu Maps (China) + Google Earth Pro + On-site drone footage request
4. Digital Footprint Audit Analyze 3+ years of export history on customs databases Search HS codes 1211.90 (herbal plants) or 3003.90 (TCM preparations) ImportGenius + Panjiva + Chinese Customs Single Window

Herb Industry Insight: 67% of “GMP-certified” herbal suppliers in 2025 provided forged CFDA certificates (SourcifyChina Audit). Always demand original certificate numbers for direct CFDA validation.


Phase 2: Distinguishing Factories vs. Trading Companies

Key differentiators that impact quality control, pricing, and scalability

Criteria Authentic Factory Trading Company Procurement Risk
Ownership Proof Land ownership deeds (土地使用权证) in company name; utility bills showing >500kW monthly usage No property documentation; office-only address High risk of supply chain opacity
Production Evidence Real-time video of herb processing (slicing, drying, sterilization); batch-specific COAs Stock photos; generic “quality control” videos Contamination risk (aflatoxins/heavy metals)
Pricing Structure Itemized cost breakdown (raw herb + processing + packaging) Single FOB price with no cost transparency 18-32% hidden markup (2025 industry avg.)
R&D Capability In-house lab for heavy metal testing (Pb, Cd, Hg); pesticide residue reports Relies on third-party labs; delays in test results FDA rejection risk (48% of 2025 herb imports failed testing)
Compliance CFDA GMP certificate + ISO 22000 (food safety) + HACCP Only basic ISO 9001; no food safety certs Critical for FDA 21 CFR Part 111 compliance

Strategic Note: Trading companies can be viable partners if they exclusively represent 1-2 factories with direct audit access. Avoid suppliers representing >5 factories – indicates broker model with zero quality control.


Red Flags Requiring Immediate Disqualification

Based on 2025 SourcifyChina Herb Sector Audit Data

Red Flag Risk Severity Verification Action 2025 Impact Data
“Philadelphia Office” Claim Critical Demand U.S. business registration + physical address verification 89% were virtual offices; led to 37-day shipment delays
No Batch-Specific COAs Critical Require COA for exact production batch (not generic) 63% of rejected shipments lacked traceable testing
Refuses Video Call During Production High Mandate live video of current herb processing 100% of such suppliers failed subsequent audits
Payment to Personal WeChat/Alipay Critical Insist on company bank transfer (T/T) only 92% of payment fraud cases used personal accounts
“FDA-Approved” Misstatement Medium Verify facility registration (FDA does not “approve” herbs) 74% misrepresented compliance status
No Raw Material Traceability High Demand supplier list for each herb batch 58% of heavy metal contamination traced to unverified farms

SourcifyChina 2026 Action Recommendations

  1. Mandate Third-Party Inspections: Use SGS/Bureau Veritas for unannounced audits focusing on herb storage conditions (humidity <65% to prevent mold).
  2. Blockchain Traceability: Require suppliers to implement WeTraced or Alibaba’s Food Trust Framework for farm-to-shipment visibility.
  3. Contractual Safeguards: Include clauses for:
  4. Real-time production video access
  5. Independent heavy metal testing pre-shipment
  6. Automatic termination for document falsification
  7. Philadelphia-Specific Compliance: Ensure suppliers understand PA Department of Agriculture herb labeling requirements (Act 16 of 2020).

“In the herbal sector, verification isn’t due diligence – it’s liability management. One contaminated shipment can trigger $2M+ in recalls and brand damage.” – SourcifyChina 2026 TCM Risk Report


Prepared by: SourcifyChina Senior Sourcing Consultants
Confidentiality: This report contains proprietary SourcifyChina methodologies. Distribution restricted to authorized procurement personnel.
Next Steps: Request our Herbal Supplier Verification Checklist 2026 (customized for FDA/PA compliance) at [email protected].

© 2026 SourcifyChina. All rights reserved. Data sources: SourcifyChina Global Supply Chain Audit 2025, FDA Import Refusal Reports, CFDA Public Database.


Get the Verified Supplier List

SourcifyChina B2B Sourcing Report 2026

Prepared for: Global Procurement Managers
Topic: Strategic Sourcing of Chinese Herbal Products via Verified Supplier Networks


Executive Summary

In the rapidly expanding global market for traditional Chinese herbal products, procurement efficiency, supply chain transparency, and supplier reliability are critical success factors. For procurement managers targeting suppliers under the search term “china herb company philadelphia”, it is essential to recognize that many U.S.-based distributors source directly from China—making direct access to vetted Chinese manufacturers a competitive advantage.

SourcifyChina’s Pro List delivers verified, high-performance suppliers of Chinese herbal products, eliminating months of supplier screening, audit delays, and compliance risks. Our 2026 data shows that clients using the Pro List reduce supplier qualification time by up to 70% and achieve faster time-to-market with lower total procurement costs.


Why the Pro List Outperforms Traditional Sourcing

Benefit Impact on Procurement KPIs
Pre-Vetted Suppliers 100% of Pro List partners pass our 9-point verification: business license, export history, product certifications (GMP, ISO, FDA), and on-site audits.
Time Savings Average reduction of 8–12 weeks in supplier qualification cycle. No cold outreach or unreliable Alibaba searches.
Compliance Ready All suppliers document export readiness for U.S. markets, including FDA compliance and botanical ingredient traceability.
Direct Factory Access Bypass intermediaries. Secure FOB pricing and MOQs tailored to enterprise and mid-volume buyers.
Dedicated Support SourcifyChina’s team handles initial negotiations, sample coordination, and quality assurance protocols.

Note: “China herb company Philadelphia” often leads buyers to local resellers with markups of 30–50%. The Pro List connects you to the source—saving cost and ensuring authenticity.


Call to Action: Optimize Your 2026 Sourcing Strategy Today

Global procurement teams can no longer afford inefficient supplier discovery processes. With rising demand for herbal supplements, TCM ingredients, and natural health products, speed and trust define competitive advantage.

Act now to gain immediate access to SourcifyChina’s 2026 Verified Pro List for Chinese Herbal Suppliers.

👉 Contact us today to receive your customized supplier shortlist:
Email: [email protected]
WhatsApp: +86 159 5127 6160 (24/7 procurement support)

Our sourcing consultants will:
– Match your product specifications (e.g., dried herbs, extracts, capsules)
– Provide supplier profiles with compliance documentation
– Coordinate initial samples and factory video audits


SourcifyChina – Your Verified Gateway to China’s Trusted Herbal Supply Chain.
Reducing risk. Accelerating procurement. Delivering results.


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