Tianjin Huilong Biotechnology Co., Ltd.
Tianjin Huilong Biotechnology Co., Ltd.
Ranking:
Supplier Assessment:
Country / Region:
China
Response time:
≤24 h
Response Rate:
High
Business Type:
Online Seller, Agent, Exporter, Manufacturer, Trading Company
Years with Global Sources:
1 year
Export Markets:
Western Europe, North America, Mid East/Africa, Eastern Europe, Central/South America, Australasia, Asia
1 year
Company Profile
Company Overview
Over 15 years of experience in peptide R&D and manufacturing
High purity: 99%|Fast delivery|After-sales service guaranteed
COA-Compliant Peptide Manufacturer
We are a COA-compliant peptide manufacturer based in China, with an integrated industrial chain, a rigorous quality control system, and a stable raw material supply chain serving global nutrition, sports supplement, and health brands. We are currently seeking exclusive distributors or agents in target markets such as the US, UK, and Brazil to expand our peptide product line. Our core portfolio covers a full spectrum of research-grade peptides for recovery and metabolic support. A complete product catalog is available upon request.
Why Partner with Us
- Complete GMP and quality system; COA, HPLC, and MS test reports available for every batch.
- Factory-direct sales with highly competitive prices and flexible minimum order quantities.
- Custom formulation, OEM, and formulation development support available.
- Stable mass production capacity and on-time global delivery.
- Exclusive regional protection and dedicated marketing support.
Be Our Partner Now
We are happy to discuss distribution terms, pricing, sample availability, and market access plans with you. To get started, please let us know your target market, business scope, and estimated sales volume. We will promptly send you our complete product catalog, detailed specification sheets, and a tailored distribution proposal. We look forward to building a long-term, mutually beneficial partnership with you.
Basic Information
Total Capitalization
US$5,000,000 to 5,999,999
Year Established
2020
Total Employees
60 to 79
Company Certificate
NA
Product Certificate
NA
Business Type
Trading Capabilities
Total Annual Sales
US$8,000,000 to 8,999,999
Export Percentage
90 percent to 94 percent
OEM Service
Yes
Small Orders Accepted
Yes
Brand Names
NA
Payment Terms
NA
Main Competitive Advantages
Experienced R&D Department, OBM (Own Branding & Manufacturing), ODM (Original Designing & Manufacturing), OEM Capability, Production Capacity, Reputation
Other Competitive Advantages
NA
Major Customer
NA
Export Markets
Business Registration Details
Registered Company
天津汇龙生物科技有限公司
Registration Number
91120103MA82QHM60Y
Company Registration Address
天津市河西区东江道南侧青林大厦3/4-1403
* In China, company names and addresses are registered in Chinese only.
Production Capacity
Factory Information
Factory Size
10000 Square Metre
No. of Production Lines
5
Number of Production Staff
80 to 99
Number of QC Staff
10 to 19
Year Established
2020
Number of R & D Staff
20 to 29
Address
High-tech Intelligent Industrial Park, Hexi District, Tianjin, China
Other Production Capacity
Site Advantages
1. Located at the core of a beauty industry cluster, offering comprehensive one-stop upstream and downstream supply chain support;
2. Surrounded by a multi-dimensional transportation network, ensuring efficient and cost-effective inbound raw material delivery and outbound finished product shipping;
3. Strategically connected to key domestic consumer markets, with close proximity to airports, expressways, and logistics hubs;
4. Benefits from a strong industrial agglomeration effect, featuring complete supporting services for raw materials, packaging, testing, and warehousing.
Quality Control
Other Quality Control
Description of Quality Control/Technical Support Department
We have established a comprehensive, standardized quality control system that ensures rigorous oversight at every stage, from raw material intake and in-process inspections to the testing of semi-finished and finished products. Equipped with professional instrumentation and microbiological analysis, we strictly control key specifications for peptide raw materials and small-format glass-vial formulations. All samples are retained, and testing data is fully traceable, ensuring consistent product quality and regulatory compliance.
Quality Control Procedures
The Quality Management Department operates an independent, standardized QC testing laboratory equipped with a full suite of precision instruments, including high-performance liquid chromatography systems, analytical balances, and constant temperature incubators, and is staffed by certified quality control professionals.
A comprehensive, end-to-end quality control process is implemented: incoming inspections are conducted on peptide raw materials and packaging materials; real-time inspections monitor the production environment and equipment cleanliness.
R&D Capabilities
Other R&D Capabilities
Procedures and Practices
A comprehensive set of standardized procedural documents has been established for the production of peptide raw materials and small-vial formulations. These cover eight core processes: raw material incoming inspection, synthesis and production operations, control, dispensing and filling, testing, finished product retention sampling, non-conforming product handling, and warehouse management, and clearly define operational steps, acceptance criteria, and equipment operating procedures. These have been formalized into written Standard Operating Procedures.
Business Registration Profile
by SGS
The supplier information below has been obtained from relevant government agencies in the supplier's country and is subject to change without prior notice. Business Registration Profile verification procedures were conducted by SGS, a third-party credit agency
Read DisclaimerRegistered Address
Room 1403, Building 3/4, South Side of Dongjiang Road, Hexi District, Tianjin City
Incorporation Date
2026/06/29
Legal Form
Limited liability company (sole proprietorship of natural person)
Company Status
Live
Registration Agency
Market Supervision Administration of Tianjin Hexi District Municipality
Registration No.
91120103MA82QHM60Y
Authorized Capital
RMB1,000,000
Paid-Up Capital
NA
Import & Export License
No
Legal Representative
Zhen Zhichao
Business Scope
General business items are: technical services, technology development, technical consulting, technical exchange, technology transfer, and technology promotion; sales of daily necessities; sales of Class I medical devices; import and export of goods; import and export of technology; wholesale of sporting goods and equipment; internet sales (excluding goods requiring a license); retail of sporting goods and equipment; sales of chemical products (excluding licensed chemical products); grain purchasing; sales of daily general merchandise; sales of textiles and raw materials; retail of shoes and hats; sales of bags and luggage; retail of cosmetics; sales of personal hygiene products; sales of maternity and baby products; advertising design and agency; advertising production; advertising placement; marketing planning; health and wellness services (non-medical); health consultation services (excluding medical services); household services; cultural and entertainment brokerage services; sales of pre-packaged health food products; sales of food additives; domestic freight forwarding; sales of toys; sales of metal products; retail of hardware products; retail of bicycles and spare parts; wholesale of bicycles and spare parts. (Except for items that require approval according to law, business activities can be carried out independently with a business license in accordance with the law.) The permitted business items are: internet information services; category II value-added telecommunications services; online data processing and transaction processing services (commercial e-commerce); sales of computer information system security products; online cultural business. (Projects that require approval according to law can only be carried out with the approval of relevant departments. Specific business projects shall be subject to the approval documents or licenses of relevant departments.)
Business Permit Expiry
Shareholders
Zhen Zhichao
Newsroom
Dedicated to Peptide Excellence and Strict Quality Control: Tianjin Huilong Bio Builds Core Strength in Biological Raw Materials
Amid the rapid growth of the cosmetic ingredient sector, market demand for peptide ingredients continues to rise; however, issues such as inconsistent purity, non-standardized packaging specifications, and weak quality control have long hindered the industry's development. Tianjin Biotechnology Co., Ltd., based in Tianjin, focuses on the R&D and packaging of peptide ingredients. By implementing a comprehensive system covering management, R&D, and quality control, the company has charted a path toward standardized and refined development.
Management
Standardized and refined enterprise management system
The company has established a comprehensive organizational structure and implemented end-to-end management systems covering HR, production, quality control, warehousing, and safety. Supported by standardized operating procedures and management practices such as on-site inspections, personnel training, and traceability record-keeping, the company ensures efficient, compliant, and stable operations.
OEM/ODM
Factory OEM/ODM Capabilities
The company possesses comprehensive, one-stop capabilities for peptide products, offering customized formulations, specifications, and packaging. Backed by an in-house R&D laboratory and technical team, we support everything from small-scale sampling (e.g., vials of peptide raw materials) to mass production. Our Class 100,000 facilities are equipped with automated synthesis, dispensing, and filling systems, supported by rigorous end-to-end quality control. We handle orders ranging from small-batch trials to large-scale production, while providing a full-service chain.
Number of Production Lines
null
Years of OEM/ODM Experience
null
Monthly Capacity
40,000 to 49,999 Boxes
Monthly Output
3,000 to 3,999 Boxes
Minimum Order
1 to 99 Boxes
Major Markets Served
Eastern Europe, Asia, North America, Mid East/Africa, Australasia, Western Europe, Central/South America
Company Profile
Introduction to the Quality Management Department
As the core department for quality control, the Quality Management Department comprises four specialized teams: Incoming Material Inspection, In Process Inspection, Finished Product Testing, and Retained Sample Management, supported by a Class 10,000 clean testing laboratory and a full suite of precision testing equipment. The department has established comprehensive inspection standards and Standard Operating Procedures to conduct full-scope incoming inspections on peptide raw materials, glass vials, and sealing components. During production, regular checks are performed on the environment, the filling process, and equipment cleanliness. Finished vials undergo sampling tests for active ingredient content, microbial limits, leakage, and visual appearance; only those that pass inspection are released. All batch samples are retained, and testing reports and production records are systematically archived. Furthermore, a process for the segregation and disposal of non-conforming products is in place, ensuring comprehensive mitigation of quality risks from source to finished product and safeguarding the fundamental safety of the products.
Introduction to the Technical Support Department
The Technical Support Department comprises a team of experts in R&D and process engineering, dedicated to three core functions: process development, on-site technical implementation, and customer technical service. Internally, the team continuously optimizes processes for peptide synthesis, purification, and small-dose dispensing; it tackles industry-wide challenges such as uneven filling and sealing leakage in glass vials while providing on-site guidance on standardized operations, equipment calibration, and troubleshooting. Externally, the department offers customized peptide formulations and purity specifications based on client needs, alongside support services such as sample preparation, stability testing, regulatory documentation, and third-party testing coordination. By leveraging its technical expertise to empower production and fully supporting clients throughout the new product development, the department ensures stable manufacturing operations and fosters long-term customer partnerships.
Overview of Departmental Functions
Integrated Quality Control and Technical Management Content
The Quality Management Department is responsible for comprehensive testing across the entire process, covering raw materials, production, and finished goods and strictly controls all specifications for bottled peptide products, while maintaining complete records and sample retention. The Technical Support Department focuses on peptide formulation R&D and the optimization of fill-and-finish processes, while also providing production guidance and customized technical services to clients, thereby ensuring quality across both internal production and contract manufacturing operations.
Corporate Core Departmental System
Quality Management and Technical Support System
The company has established two core functional departments, Quality Management and Technical Support, creating an operational model underpinned by "technical R&D foundations" and "comprehensive quality control." The Quality Management Department operates an independent, standardized QC laboratory equipped with a full suite of precision testing instruments; it implements a three-tier inspection process covering incoming raw materials, the production process, and finished goods, conducting comprehensive testing (including purity, microbial limits, and seal integrity) on peptide glass vial products while maintaining batch retention samples and detailed records to ensure full product traceability. Comprising peptide R&D specialists and process engineers, the Technical Support Department focuses on formulation development and the optimization of fill-and-finish processes, overcoming production challenges such as leakage and content inconsistency in small-format glass vials; the department provides internal guidance on standardized production while offering external services including custom formulation, prototyping, and technical consultation thereby ensuring product stability and regulatory compliance through a combination of technical innovation and rigorous quality control.
Introduction to Functional Departments
Safeguarding Quality Control Empowering Through Technology Content
The company has established two core functional departments, Quality Management and Technical Support, creating a dual-guarantee operational model underpinned by technical R&D and comprehensive quality control.
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