What is the minimum order quantity (MOQ)?

The minimum order quantity is 1 set.

Does the manufacturer offer OEM or ODM services?

Yes, both OEM and ODM services are available with full customization options.

Marya Pharmaceutical Large-Volume Parenteral (LVP) Preparation System for Liquid Medicine

Name: Marya Pharmaceutical Large-Volume Parenteral (LVP) Preparation System for Liquid Medicine
Brand: Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.
SKU: 2188639375

Shanghai, ChinaShanghai Marya Pharmaceutical Engineering & Project Co., Ltd.

US$50,000.00

1 Piece

US$40,000.00

2+ Pieces

Product profile

Customization

Available

Application

Biotechnology Industry, Chemical industry, Clinical Diagnosis, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry

Capacity

20000 L/hr

Model NO.

MY-PS

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

Filtration, Ultrafiltration

Warranty of core components

1 Year

Tank Material

Stainless Steel 316L

Temperature Resistance

150℃

Working Volume

2~15000L

Weighing Control Accuracy

Power Supply

380V 50Hz

Sealing and Protection Levels

IP65

Temperature Control Accuracy

Temperature Range-10~150℃ ±0.2℃

Stirring Speed Control Accuracy

Speed Range 0~450rpm ±3.0%

Pressure Control Accuracy

Pressure Range-0.01MPa~0.06MPa ±0.01MPa

Transport Package

Wooden Box

Specification

350*180*300

Trademark

Marya

Origin

China

Key features

GMP & ASME BPE Compliant: Fully integrated system designed to meet GMP and ASME BPE standards for pharmaceutical manufacturing.

Fully Automatic Control System: One-key CIP/SIP operation with recipe management, electronic signatures, and audit tracking.

Wide Application Versatility: Suitable for small molecules, complex preparations (liposomes), and biological products (antibodies).

Customizable Working Volume: Flexible tank sizes ranging from 2L to 15000L to suit various production scales.

Multi-Industry Certification: Certified by CE, FDA, GMP, and ISO, meeting EU PED requirements for global compliance.

Company profile

Flexible CustomizationProduct CertificationYears of Export ExperienceR&D Capabilities

Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Full Customization, Flexible customization CertifiedExport Year: 12 Years CertifiedNearest Port: Shanghai Port; Ningbo PortAverage Response Time: ≤4.44h

About Our Factory & Business Background

AddressNo211, North Fute Road, Pudong Area, 200131, Shanghai, China

Plant Area3210 square meters

Number of Employees69

Terms of PaymentLC, 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 TimePeak Season Lead Time: 1-3 months Off Season Lead Time: one month

Minimum Order Quantity1 Set

Supply Chain Partners150

Our Production Capability & Technical Expertise

Main ProductsPharmaceutical Filling Line, Cleanroom Project

Production Lines6

Production MachinesWelding Machine, Lathe, Milling Machine, Bench Drill

QA/QC inspectors3 people

Inspection Type for Finished Products100% inspection(Visual inspection & Function inspection)

Inspection Method for Finished ProductsHave instructions and uniformly followed

R&D Engineers30 people

Traceability of Raw MaterialsYes

Our Industry Experience & Global Business Record

Year of Establishment2014-03-10

Main MarketsNorth America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe

Repeat Buyers Choice10%~30%

Number of Foreign Trading Staff16

Overseas Agent/BranchNo

New Products Launched in Last yearYes

Our Certifications, Standards & Industry Recognition

Product CertificationCE

Cooperated with Fortune 500Yes

Product Q&A

Q:What types of pharmaceutical preparations can this system handle?

It supports general small molecules, complex preparations like suspensions and liposomes, and biological products such as antibodies and vaccines.

Q:What is the working volume capacity of the system?

The system offers a flexible working volume ranging from 2 liters to 15,000 liters.

Q:Is the system fully automatic and compliant with GMP?

Yes, it is a fully automatic, GMP-engineered solution with ASME BPE design, featuring one-key CIP/SIP and electronic record tracking.

Q:What certifications does the equipment hold?

The system holds CE, FDA, GMP, and ISO certifications and meets EU PED requirements for pressure equipment.

Q:What is the warranty period for core components?

The warranty for core components is 1 year.

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