Marya Pharmaceutical CIP/SIP Capability Liquid Preparation Skid with Automated Formulation
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Product Attributes
- Customization
- Available
- Application
- Biotechnology Industry, Chemical industry, Clinical Diagnosis, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry
- Capacity
- 20000 L/hr
- Certification
- CE, FDA, GMP, ISO
- Control System
- Fully Automatic
- Treatment Process
- Filtration, Ultrafiltration
- Warranty of core components
- 1 Year
- Power Supply
- 380V 50Hz
- Tank Material
- Stainless Steel 316L
- Weighing Control Accuracy
- 3%
- Sealing and Protection Levels
- IP65
- Temperature Control Accuracy
- Temperature Range-10~150℃ ±0.2℃
- Stirring Speed Control Accuracy
- Speed Range 0~450rpm ±3.0%
- Temperature Resistance
- 150℃
- Transport Package
- Wooden Box
- Specification
- 350*180*300
- Trademark
- Marya
- Origin
- China
- Package Size
- 350.00cm * 180.00cm * 300.00cm
- Package Gross Weight
- 3500.000kg
Shipping
- Shipping Cost:
- Contact the supplier about freight and estimated delivery time.
Online Trading Protection
- Payment Guarantee
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Platform-protected payments with refund support for eligible order issues.
- Platform Logistics
- Clearer shipment tracking with platform-supported logistics.
- Inspection Service
- Optional pre-shipment inspection for quality and quantity checks.
- After-Sales & Dispute Handling
- Platform-assisted dispute resolution, including refunds or returns when applicable.
Only orders placed and paid through Made-in-China.com Secured Trading are eligible for payment protection and the corresponding platform services.
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Product Description
Introduction
The Maya Pharmaceutical Formulation Skid is a precision drug preparation equipment designed for the mixing and dispensing of liquid pharmaceuticals. It enables the controlled addition of active pharmaceutical ingredients into solvents such as Water for Injection (WFI), followed by homogenization through stirring, heating, sterilization, and filtration processes to achieve the desired drug concentration.
This system is widely used in both sterile and non-sterile pharmaceutical manufacturing, including applications in biopharmaceutical production, large-volume parenteral (LVP) solutions, and other critical drug formulation processes.
Classification
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General Formulation System
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For small-molecule chemical prep (e.g., aqueous injections, lyophilized powder injections).
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Complex Formulation System
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Handles advanced processes: suspensions, emulsions, liposomes, microspheres.
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Biological Formulation System
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For biotech products (antibodies/vaccines/blood products/recombinant proteins) & auxiliary liquids (media/buffers).
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1) Modular Design - Cost-Saving & Efficient
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Pre-tested modular equipment reduces installation costs, accelerates delivery, and ensures flexibility.

2) Fully Automated Operation - Smart & Compliant
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1-click CIP/SIP with auto-detection for cleaning/sterilization completion.
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Computerized features: Recipe management, e-signature, e-records, and audit trail for full automation.

3) Process Control & Real-Time Monitoring
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Critical parameter control (temp, DO, pH) with auto-alerts for deviations to ensure drug quality.

4) 3D Simulation & Ergonomic Layout
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Pre-production 3D modeling optimizes piping, valve, and instrument placement for user-friendly operation.

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Premium Material & Compliance
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316L stainless steel tanks (2L-12,000L) with electrolytic polishing (Ra<0.4µm), ensuring cleanability and compliance with EU PED & FDA standards.
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FDA-compliant connections (clamps/NA) and seals (EPDM/PTFE), with PTFE gaskets for jacket nozzles.
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Sterility Assurance
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Sterile ventilation/exhaust filters and CIP spray balls for aseptic operations.
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Optional sterile double-tube plate heat exchanger for WFI cooling and filter integrity testing.
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Safety & Control Systems
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Integrated safety devices (burst disc/safety valve + pressure gauge) for equipment/personnel protection.
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Precision temperature (bottom probe) and pressure (top probe) monitoring with automated controls.
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Efficient Mixing & Heat Transfer
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Magnetic stirrer (bottom, electromagnetic-driven) or mechanical stirrer (top), both with variable frequency speed regulation.
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Accurate Material Handling
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Weighing/liquid-level detection for controlled water addition and material feeding.
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High-Performance Filtration
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Sterilization-grade PES filters (pH 1-14, 150°C resistant) with organic solvent compatibility and reliable bacterial retention.
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Operational Visibility
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Illuminated sight glasses for real-time level monitoring.
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| Name | Parameters |
| Working volume | 2~15000L |
| Material | 304, 316L, 904L, TA2 |
| Stirring type | Upper mechanical, lower magnetic stirring |
| Stirring speed control accuracy | Speed range 0~450rpm ±3.0% |
| Temperature control accuracy | Temperature range-10~150ºC ±0.2ºC |
| Pressure control accuracy | Pressure range-0.01Mpa~0.06Mpa ±0.01MPa |
| Weighing control accuracy | 3‰ |
| Power supply | 380V 50Hz (Note: Other voltages require a transformer) |
| Sealing and protection levels | IP65 |



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
With 12 years of industry experience, we have independently developed a comprehensive range of filling lines, including vial, pre-filled syringe (PFS), and cartridge filling lines. In addition, we offer self-developed supporting equipment such as isolators, solution preparation systems, and water treatment systems. Our capabilities also extend to providing turnkey solutions for cleanroom projects and complete filling production lines. Centered around professional filling line technology, we are committed to delivering aseptic production lines and solutions that are stable, compliant, and efficient.
With branch offices located in Shanghai, Hong Kong, Osaka, Changsha, and Guangzhou. With three factories and a team of experts and technicians boasting over 20 years of experience in the pharmaceutical and medical industries, Marya has successfully partnered with pharmaceutical companies and governmental authorities in 60 countries.
Our expertise encompasses factory construction and securing GMP and FDA certifications. We are dedicated to our clients' success, ensuring they enjoy a worry-free and satisfying experience. Our commitment lies in helping clients design and provide high-standard customized aseptic pharmaceutical engineering solutions.
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 60+ 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 60+ countries of 6 continents including the United States, Britain, Australia, Malaysia, Argentina and Tanzania to bulid 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
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Business Type
- Manufacturer/Factory & Trading Company
- Address
- China(Shanghai) Pilot Free Trade Zone, North Fute Road, No. 211, 302 Parts, Room 368, Shanghai, China
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Plant Area
- 3210 square meters
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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
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Average Lead Time
- Peak Season Lead Time, 1-3 months, Off Season Lead Time, one month
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Nearest Port
- Shanghai Port; Ningbo Port
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Minimum Order Quantity
- 1 Set
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Supply Chain Partners
- 150
Our Production Capability & Technical Expertise
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Main Products
- Pharmaceutical Filling Line, Cleanroom Project
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Production Lines
- 6
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Production Machines
- Welding Machine, Lathe, Milling Machine, Bench Drill
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Inspection Type for Finished Products
- 100% inspection Visual inspection Function inspection
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Inspection Method for Finished Products
- Have instructions and uniformly followed
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Customization Options
- Full Customization,Flexible customization
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ODM Service Available
- Yes
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OEM Service Available
- Yes
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R&D Engineers
- 1 people
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Traceability of Raw Materials
- Yes
Our Industry Experience & Global Business Record
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Year of Establishment
- 2014-03-10
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Export Year
- 12 Years
- Main Markets
- North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe
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Repeat Buyers Choice
- 10%~30%
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Number of Foreign Trading Staff
- 16
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Overseas Agent/Branch
- No
Our Certifications, Standards & Industry Recognition
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Product Certification
- CE
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Cooperated with Fortune 500
- Yes
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