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KS Nutripharma supplements contract manufacturer

Supplement Manufacturer for OEM & ODM Projects

Since 2007, KS NUTRIPHARMA® has supported supplement brands and distributors with formulation development, ingredient sourcing, and commercial manufacturing across multiple dosage forms.

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KS Nutripharma® Group Overview

19+
Years Experience
260+
Employees
2
R&D Centers
7
Certificates
81000+
㎡ Production Facility
5
Manufacturing Bases
5
Raw Material Lines
7
Supplement Lines
2+
Million Softgels / Day
5+
Million Capsules / Day
12+
Million Tablets / Day
2.5+
Million Gummies / Day
5000+
Tons Raw Material Capacity
4
Cultivation Bases
60+
Exported Countries
500+
Global Brands

Supplement Manufacturing Built For OEM/ODM Projects

KS NUTRIPHARMA® Group is a supplement manufacturer supporting brands, distributors, and nutraceutical companies with formulation development, ingredient sourcing, and commercial production.

Founded in 2007, KS Nutripharma has supported more than 500 nutraceutical brands and distributors across international markets. Our manufacturing capabilities cover capsules, tablets, softgels, gummies, powders, and liquid supplements, with in-house R&D support for formulation and product development.

Rather than treating formulation, raw materials, and manufacturing as separate steps, our teams coordinate these requirements as part of the same OEM/ODM project. Depending on the product, this may include reviewing ingredient specifications, assessing dosage-form feasibility, developing samples, coordinating raw materials, transferring the formula to production, and completing finished-product testing and batch documentation.

Core Manufacturing Capabilities

  • Capsules — hard-shell and vegetarian capsule manufacturing
  • Tablets — standard and coated tablet production
  • Softgels — oil-based and suspension formulations
  • Gummies — functional and botanical gummy production
  • Powders & Granules — powder blending, granulation, and stick-pack filling
  • Liquid Supplements — liquid formulation and manufacturing

The appropriate manufacturing route depends on the formula, ingredient characteristics, target dosage, dosage form, packaging, and market requirements. These factors are reviewed as part of the product development and manufacturing process.

Development History-From Botanical Ingredients to Supplement Manufacturing

2007 — Shaanxi Kingsci Biotechnology Co., Ltd.-Botanical Ingredient Production
Shaanxi Kingsci Biotechnology Co., Ltd. was established in Xi'an in 2007, with an initial focus on botanical ingredients and plant extract production. The company began with botanical extraction capabilities, including a lutein monomer extraction line. This early focus established the group's experience in plant-based raw materials, extraction, separation, and ingredient processing. Today, Shaanxi Kingsci continues to operate as a botanical ingredient manufacturer, with products including lutein, astaxanthin, ecdysterone, and other plant-based extracts.
2014 — Xi'an H&Y Biotechnology Co., Ltd.-R&D and Technical Development
Xi'an H&Y Biotechnology Co., Ltd. was established in 2014 as the group expanded its technical and international business capabilities. A dedicated R&D function was developed alongside the company's ingredient business, supporting work in botanical extraction, separation, purification, and product development. This stage expanded the group's capabilities beyond ingredient supply toward technical support for customized nutraceutical projects.
2017 — GAP-Certified Botanical Cultivation-Upstream Raw Material Development
In 2017, the group began developing GAP-certified cultivation bases for selected botanical raw materials. The cultivation program includes botanical sources such as marigold, Panax notoginseng, Haematococcus pluvialis, and Cyanotis arachnoidea. For these selected materials, upstream cultivation provides an additional level of control over the sourcing and harvesting stages before extraction and ingredient processing.
2019 — Shanyang H&Y Biotechnology Co., Ltd.-Manufacturing Capacity Expansion
Shanyang H&Y Biotechnology Co., Ltd. was established within the Shanyang Traditional Chinese Medicine Industrial Park. A modern production facility was built, equipped with advanced extraction and natural ingredient processing lines to support large-scale manufacturing.
2021–Present — Expansion into OEM/ODM Supplement Manufacturing
The group's capabilities subsequently expanded from botanical ingredients into finished dietary supplement manufacturing. Today, KS NUTRIPHARMA® supports OEM/ODM projects across capsules, tablets, softgels, gummies, powders, granules, and liquid supplements, together with formulation development, quality control, testing, packaging, and export coordination. This development allows the group to support projects at different stages—from customers sourcing a defined botanical ingredient to brands requiring a complete finished-product manufacturing program.
2023 — Los Angeles Warehouse-North American Logistics
In 2023, KS Nutripharma established a warehouse in Los Angeles to support North American customers and supplement its international logistics network. The facility provides a local logistics point for customers in the U.S. West Coast market.
2024 — New Jersey Warehouse & Los Angeles Office-Additional U.S. Support
In 2024, KS expanded its U.S. presence with a New Jersey warehouse and a Los Angeles office. The additional location provides a second U.S. logistics point, while the Los Angeles office supports communication and coordination with North American customers. These facilities complement the group's manufacturing and export operations in China rather than replacing the core manufacturing and quality-control functions performed at the production sites.

Integrated Manufacturing Ecosystem

Our production system integrates the full nutraceutical value chain:

Raw Material Cultivation → Extraction → Formulation → Manufacturing → Testing → Packaging → Export

This integrated structure allows:

  • Consistent raw material quality
  • Stable batch-to-batch production
  • Faster product development cycles
  • Full traceability for global compliance
Integrated Manufacturing Ecosystem
Advanced Delivery & Dosage Form Technologies

Advanced Delivery & Dosage Form Technologies

We provide industrial-scale capabilities across multiple advanced formulation systems:

  1. Liposomal Technology: used to enhance absorption of fat-soluble and sensitive actives
  2. Microencapsulation Technology: used for controlled release and stability protection.
  3. Capsule-in-Capsule Technology: advanced dual-release system for multi-stage absorption.
  4. Instant & Soluble Powder Systems: designed for beverage and functional nutrition markets.
  5. Microgranule & Beadlet Systems: used for controlled release and stability-sensitive ingredients.

R&D & Product Development Support

Our 2 R&D centers support formulation innovation for:

  • Longevity supplements
  • Immunity support supplements
  • Digestive support supplements
  • Cognitive health formulas
  • Women’s & men’s health products
  • Beauty from within supplements
  • Eye health supplements
  • Botanical extract formulations

We support:

  • Custom formulation development
  • Ingredient compatibility optimization
  • Stability testing
  • Pilot-to-scale production transfer
R&D & Product Development Support
Integrated Quality Control & Testing System

Integrated Quality Control & Testing System

Our QC system operates across every production stage:

  • Raw material identity verification (HPLC/UV testing)
  • In-process quality monitoring
  • Finished product stability testing
  • Microbiological safety testing
  • Heavy metal and contaminant screening

All batches are released with COA documentation for global compliance.

Certifications & Compliance System

All products are manufactured under strict international standards:

  • GMP-certified production system
  • ISO / HACCP / FSSC compliance
  • HALAL & KOSHER certified production options
  • Batch testing with COA documentation
  • Heavy metal & microbiological testing

Ensures regulatory readiness for US, EU, and global markets.

Certificates & Compliance System
Global Supply Chain & Logistics

Global Supply Chain & Logistics

To support global supplement brands, we provide:

  • US West Coast warehouse (Los Angeles)
  • US East Coast warehouse (New Jersey)
  • Export coverage to 60+ countries
  • Fast logistics support for different markets

Intellectual Property Protection System

KS Nutripharma provides strict IP protection for global brand partners.

Our system includes:

  • Formula confidentiality agreements (NDA-based manufacturing)
  • Dedicated production segregation for private label clients
  • Restricted-access formulation database
  • Batch-level traceability control
  • IP-safe formulation development workflows

This ensures brand formulations remain fully protected throughout the manufacturing lifecycle.

Intellectual Property Protection
Integrated GAP-Certified Cultivation System

Integrated GAP-Certified Cultivation System

Our raw material supply chain is supported by GAP-certified cultivation bases, ensuring upstream consistency and traceability.

These cultivation systems cover key botanical ingredients including:

  • Marigold (lutein raw material)
  • Panax notoginseng
  • Haematococcus pluvialis (astaxanthin source)
  • Cyanotis arachnoidea

System advantages:

  • Controlled agricultural conditions
  • Standardized harvesting cycles
  • Reduced contamination risk
  • Stable active compound content

This upstream control ensures consistency from cultivation to finished supplement production.

KS Nutripharma softgel production new line
Softgel Production New Line
KS Nutripharma liquid supplement new line
Liquid Supplement Production New Line
KS Nutripharma extract workshop2
Hard Capsule Production New Line
KS Nutripharma extract workshop2
Plant Extract Line-Crude
KS Nutripharma -kaikang production base
Plant Extract Line-Purify
KS Nutripharma Research and Develeopment Center1
R&D Testing Center1
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