Marya China Aseptic Pw/Wfi Treatment and Distribution System Factory
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Product Highlights
- GMP and FDA Compliance: Adheres to cGMP, ISPE, and FDA standards for reliable pharmaceutical water handling.
- High Salt Rejection Rate: Achieves 99.5% salt rejection rate ensuring high purity water quality.
- Full Customization Options: Offers full and flexible customization for usage, materials, and system design.
- Automated CIP and SIP Control: Fully automatic control of Clean-in-Place and Sterilize-in-Place processes.
- Electronic Reporting and Audit: Automatically generates electronic reports with audit tracking and intelligent maintenance.
- Modular Compact Design: Features PW/WFI modular design with compact structure for easy operation.
- Comprehensive After-Sales Service: Includes field installation, commissioning, and training services.
- Integrated Multi-System Solutions: Designs integrated solutions for water, pure steam, compressed air, and nitrogen.
Product Attributes
- Customization
- Available
- Certification
- CE, GMP
- Salt Rejection Rate
- 99.5%
- Model NO.
- MY-WS
- Application
- Industry
- Capacity
- 400 Gallon
- Usage
- Pw & Wfi System
- Core Components
- RO Systems or EDI Systems
- Material
- Stainless Steel
- Qualification Documents
- Dq, Iq, Oq, Pq
- After-Sales Service
- Field Installation, Commissioning and Training
- Typical Waste Disposal Ratio
- 2-8 %
- Gas Pressure Output Range of Pure Steam
- 2-5
- Transport Package
- Wooden Case Packaging
- Specification
- Customized
- Trademark
- MARYA
- Origin
- China
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Product Description
Introduction
Marya China's Aseptic PW/WFI Treatment and Distribution System Factory offers top-notch solutions. Our system adheres to cGMP, ISPE, and FDA standards, ensuring reliable PW/WFI handling. It's a crucial part of pharma and biotech industries, precisely treating and distributing both Purified Water and Water for Injection. With strict sterility controls, we provide a high-quality water treatment and distribution system for your pharmaceutical needs.
Performance Features
(1)PW/WFI modular design with compact structure and easy operation and maintenance;
(2)Frequency conversion operation of circulating pump, and system flow design and operation in line with GMP and ISPE guidelines;
(3)Fully automatic control of CIP and SIP of storage and distribution system;
(4)Design and manufacture the integrated solutions for purified water, water for injection, pure steam, compressed air, nitrogen, etc. that meet the process requirements of pharmaceutical companies;
(5)The control system can automatically generate electronic reports and records, and has the functions of audit tracking, intelligent maintenance and remote troubleshooting.













About the Supplier
This supplier has been audited by TÜV Rheinland. Verify the report on the official TÜV Rheinland website with ID "MIC-ASR2542074". Items marked "" are certified.
Company Profile
Marya is a professional aseptic filling line manufacturer with turnkey solutions. With 12 years of industry experience, we have independently developed a comprehensive range of filling lines, including cartridge, vial, and pre-filled syringe (PFS) filling lines. In addition, we offer self-developed supporting equipment such as isolators/RABS, solution preparation systems, and water treatment systems, and VHP sterilizers. Our capabilities also extend to providing turnkey solutions for cleanroom projects and complete filling production lines. We have expanded business to over 70 countries worldwide, serving clients covering European, American and other mainstream markets, including renowned pharmaceutical enterprises and official governmental institutions. Centered around professional filling line technology, we are committed to delivering aseptic production lines and solutions that are stable, compliant, and efficient.
Five Things You Should Know About Marya
1 Engineering design
Our experienced engineering team with more than 20 years experience in pharmaceutical production plants, can ensure that process and equipment for your plant is designed and manufactured in the most cost-effective manner with reliable quality to fulfil GMP/FDA/ISO/SGS requirement.
2 Manufacturing Plants
Marya's 3 manufacturing plants for clean room walls, windows, doors and pharmaceutical machinery are all under strict quality management systems certified to ISO 9001 with a focus on continuous quality improvement.
3 Installation & Commissioning
Experienced, professional, high-efficiency and strictly stick to the schedule, our installation engineers and workers team has successfully installed more than 300+ projects in oversea with high customer satisfaction.
4 Proven Experience
Since 2014, Marya has maintained good cooperation relationship with Novartis, US pharma, MSD, NBA (Zimbabwe National Biotechnology Administration), Novo Nordisk, Techno drugs and other internationally renowned top pharmaceutical companies and national government agencies for a long time. So far, we have assisted famous pharmaceutical factories or government agencies in more than 70+ countries of 6 continents including the United States, Britain, Australia, Malaysia, Argentina and Tanzania to build high-grade cleanroom and aseptic preparation filling production lines that meet local requirements and GMP or FDA standards, winning a very good reputation.
5 Continuous Technical Support
Whatever you buy from us, No matter when your project finished, we will provide continuous service on the operation, maintenance, repairing, spare parts supplying improving and upgrading.
About Our Factory & Business Background
-
Business Type
- Manufacturer/Factory & Trading Company
- Address
- No211, North Fute Road, Pudong Area, 200131, Shanghai, China
-
Plant Area
- 3210 square meters
-
Number of Employees
- 69
- Terms of Payment
- LC, T/T, D/P, PayPal, Western Union, Small-amount payment, Money Gram
- International Commercial Terms(Incoterms)
- FOB, EXW, CFR, CIF, DDP, CIP, Others
-
Average Lead Time
-
Peak Season Lead Time: 1-3 months
Off Season Lead Time: one month -
Nearest Port
- Shanghai Port; Ningbo Port
-
Minimum Order Quantity
- 1 Set
-
Supply Chain Partners
- 150
Our Production Capability & Technical Expertise
-
Main Products
- Pharmaceutical Filling Line, Cleanroom Project
-
Production Lines
- 6
-
Production Machines
- Welding Machine, Lathe, Milling Machine, Bench Drill
-
QA/QC inspectors
- 3 people
-
Inspection Type for Finished Products
- 100% inspection(Visual inspection & Function inspection)
-
Inspection Method for Finished Products
- Have instructions and uniformly followed
-
Customization Options
- Full Customization, Flexible customization
-
ODM Service Available
- Yes
-
OEM Service Available
- Yes
-
R&D Engineers
- 30 people
-
Traceability of Raw Materials
- Yes
Our Industry Experience & Global Business Record
-
Year of Establishment
- 2014-03-10
-
Export Year
- 12 Years
- Main Markets
- North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe
-
Repeat Buyers Choice
- 10%~30%
-
Number of Foreign Trading Staff
- 16
-
Overseas Agent/Branch
- No
-
New Products Launched in Last year
- Yes
Our Certifications, Standards & Industry Recognition
-
Product Certification
- CE
-
Cooperated with Fortune 500
- Yes
FAQ
- What standards does the system comply with?
- The system adheres to cGMP, ISPE, and FDA standards to ensure reliable handling of Purified Water and Water for Injection.
- What is the salt rejection rate?
- The system achieves a salt rejection rate of 99.5%.
- Can the system be customized?
- Yes, full customization and flexible customization options are available for usage, core components, and materials.
- What is the minimum order quantity?
- The minimum order quantity is 1 set.
- What is the lead time for production?
- Lead time is one month during off-peak season and 1-3 months during peak season.
- What after-sales services are provided?
- We provide field installation, commissioning, and training as part of our after-sales service.
- What materials are used for the system?
- The system is manufactured using Stainless Steel.
- Does the system support automated reporting?
- Yes, the control system can automatically generate electronic reports and records with audit tracking functions.
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