Cheap pharmaceutical preparation System

1. This series of vessels feature heating and thermal insulation functions, and are manufactured, pressure-tested, and inspected in accordance with technical standards for steel welded vessels.

2. Available in a range of capacities from 100L to 10,000L, various specifications are offered to suit different needs. Custom designs and processing can also be provided based on actual customer requirements.

3. The mixing shaft is sealed with imported sanitary-grade mechanical seals. The reducer uses world-renowned brands such as Germany’s Flanders or SEW, with mixing speeds ranging from 36–53 rpm. Variable frequency drive control is also available.

4. The interfaces comply with the international ISO standard quick-clamp fitting system. The inner tank is constructed of imported 316L or 304 stainless steel.

5. The tank is equipped with a level gauge (non-contact ultrasonic, static pressure transmission, or glass tube type), an air breather vent, a sterilization steam outlet, a thermometer (digital or dial type), a CIP-compatible tank washer, a sight glass, multiple liquid inlet/outlet ports, and a manhole.

6. Interior material: SS316L, interior finish: 0.28 – 0.45 μm; Exterior material: SUS304 mirror-finished panel.

7. Working pressure: atmospheric; Working temperature: 60 – 100°C; Sterilization pressure: 0.15 – 0.3 MPa; Sterilization temperature: 121 – 132°C.

Automated Liquid Preparation & Formulation System for Pharmaceutical Manufacturing

Introducing our fully integrated Automated Liquid Preparation & Formulation System, a precision-engineered solution designed to streamline and standardize the compounding of buffers, media, and liquid drug products in cGMP environments. This turnkey pharmaceutical preparation system automates the entire workflow—from ingredient addition and dissolution to pH adjustment, mixing, and sterile transfer—ensuring batch-to-batch consistency, reducing operator error, and enhancing sterility assurance. We offer scalable solutions to fit every budget and scale, from a cost-effective cheap pharmaceutical preparation system for pilot-scale and R&D to comprehensive wholesale pharmaceutical preparation system packages for high-volume commercial production and multi-facility deployment.

Precision-Engineered for cGMP Compliance and Reproducibility

Our system is designed as the definitive pharmaceutical preparation system for critical processes. It integrates high-accuracy load cells, Coriolis mass flow meters, and peristaltic or sanitary pumps for gravimetric or volumetric addition of liquids and powders. Automated temperature control, inline pH and conductivity monitoring, and programmable mixing sequences ensure every parameter is precisely controlled and documented. Constructed with 316L stainless steel, sanitary fittings, and Clean-in-Place (CIP) capabilities, it meets the highest hygienic standards and supports full validation (IQ/OQ/PQ), making it ideal for producing cell culture media, fermentation buffers, and final drug formulations for injectables and biologics.

Scalable Solutions for Every Stage of Production

We recognize that needs vary from development to full-scale manufacturing. Our flexible portfolio includes:

• Entry-Level Efficiency: A streamlined cheap pharmaceutical preparation system that provides core automation—precise weighing, mixing, and transfer—at an accessible price point. Perfect for process development, clinical trial material production, and small-batch manufacturing where capital expenditure is a key consideration.

• Commercial-Grade Performance: Robust, high-capacity systems designed for 24/7 operation in commercial facilities. These systems feature larger vessel sizes, higher degree of automation, and advanced process analytical technology (PAT) integration.

• Volume-Based Value: For large manufacturers, CDMOs, or organizations equipping multiple sites, our wholesale pharmaceutical preparation system program offers significant value. This includes tiered pricing, standardized modular designs for rapid deployment, and centralized validation support, providing a consistent, compliant platform across your global operations.

Core Features & Technical Advantages

• Automated Recipe Execution: A 21 CFR Part 11-compliant PLC with an intuitive HMI allows for secure storage and hands-off execution of complex formulation recipes, ensuring reproducibility.

• Closed Processing: Utilizes closed vessels and sterile connectors to minimize operator exposure and prevent microbial or particulate contamination during ingredient addition and mixing.

• In-Process Control (IPC): Integrated sensors for real-time monitoring and adjustment of pH, conductivity, temperature, and dissolved oxygen (DO).

• Powder Handling Integration: Optional integrated powder transfer modules (e.g., split-valve systems) for safe and contained addition of API and excipients.

• Data Integrity: Complete electronic batch records with audit trails for all material inputs, process parameters, and operator actions.

Ideal Applications

• Buffer & Media Preparation: Large-scale, consistent preparation of cell culture media and chromatography buffers for biopharmaceutical processes.

• Drug Product Formulation: Compounding of sterile injectables, intravenous (IV) bags, ophthalmics, and oral liquid suspensions.

• Diagnostic Reagent Production: Precise mixing of assay buffers, calibrators, and liquid reagents.

• Process Development: Scalable platform for optimizing formulation recipes from bench to plant.

Your Partner in Process Automation & Scale-Up

We provide an end-to-end partnership, from initial process analysis and system design to fabrication, factory acceptance testing (FAT), site installation, and full commissioning & qualification (C&Q) support. Our goal is to deliver a pharmaceutical preparation system that is not just equipment, but a validated and optimized extension of your manufacturing process.