Production scale pharmaceutical filter dryer for aseptic filtration and vacuum drying

Production Scale Pharmaceutical Filter Dryer for Aseptic Filtration and Vacuum Drying (15 kg Batch)

20 µm / 800 mm chamber diameter
€0,00
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Production scale pharmaceutical filter dryer for aseptic filtration and vacuum drying

Production Scale Pharmaceutical Filter Dryer for Aseptic Filtration and Vacuum Drying (15 kg Batch)

Micron Rating
Dimensions

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Product description

A production scale pharmaceutical filter dryer is a sealed aseptic processing system designed for batch filtration, washing, dewatering, and vacuum drying of pharmaceutical solids. The system integrates multiple process stages within a single enclosed chamber to maintain sterile conditions and reduce product handling during pharmaceutical manufacturing. This type of equipment is commonly used in pilot plants and full production environments where pharmaceutical solids must be processed under controlled and contained conditions.

Technical overview

The system combines vibratory filtration with vacuum drying technology to process pharmaceutical slurries in a closed pressure vessel. Liquid-solid separation occurs on a screening surface while solids remain on the screen deck. After filtration, the retained solids can be washed and further dewatered on the screen. The system then transitions to vacuum drying while the solids are gently redistributed on the screen surface to promote uniform drying. Production-scale systems of this type are typically designed to process batches of approximately 15 kg of solids and can also be used for wet separation processes when drying is not required. :contentReference[oaicite:0]{index=0}

Operating principle

The separator operates using controlled vibratory motion applied to the screen surface within a sealed process chamber. Slurry is introduced at the top of the chamber where it spreads across the screening deck. Liquid passes through the screen openings while solids remain on the screen surface. The vibratory motion promotes drainage and keeps particles moving across the screen to prevent fouling. Following filtration and optional washing steps, vacuum drying is initiated within the chamber. A controlled flow of inert gas, typically nitrogen, is introduced beneath the product bed while the vibratory motion gently tumbles the solids. This motion promotes uniform drying and helps prevent the formation of agglomerates while moisture is removed from the product. :contentReference[oaicite:1]{index=1}

Material options

Typical construction materials include:
  • Stainless Steel 304
  • Stainless Steel 316
  • Stainless Steel 316L
Wetted parts are typically manufactured from corrosion-resistant stainless steel suitable for pharmaceutical processing environments. Internal surfaces are commonly polished to reduce contamination risk and improve cleanability.

Available micron ratings

Typical screen opening options include:
  • 20 µm
  • 25 µm
  • 32 µm
  • 38 µm
  • 45 µm
  • 53 µm
  • 63 µm
  • 75 µm
  • 90 µm
  • 106 µm
  • 125 µm
  • 150 µm
  • 180 µm
  • 212 µm
  • 250 µm
  • 300 µm
  • 355 µm
  • 425 µm
  • 500 µm
  • Custom screen opening
The selected screen opening determines the filtration cut point and influences the separation efficiency and product recovery.

Design and construction

The production scale filter dryer is designed as a sealed pressure vessel with hygienic construction suitable for pharmaceutical manufacturing. Typical design characteristics include:
  • Sealed process chamber with pressure and vacuum capability
  • Vibratory screening surface for filtration and dewatering
  • Integrated filtration, washing, and drying stages
  • Vacuum drying capability with controlled gas purge
  • Highly polished crevice-free internal surfaces
  • Clean-in-place (CIP) and sterilization capability
  • Sealed product discharge system
  • Batch processing configuration
The sealed design helps contain potent pharmaceutical compounds and improves product recovery by minimizing product losses during processing. :contentReference[oaicite:2]{index=2}

Typical applications

Typical applications include:
  • Active pharmaceutical ingredient (API) filtration
  • Pharmaceutical slurry processing
  • Crystallization filtration
  • Production-scale filter drying
  • Biopharmaceutical processing
  • Fine chemical manufacturing
  • High-purity compound processing
  • Pharmaceutical batch production

Key benefits

Key operational advantages include:
  • Integrated filtration, washing, and drying in one system
  • Closed aseptic processing environment
  • Reduced product handling and transfer
  • Improved containment of potent pharmaceutical compounds
  • Uniform vacuum drying performance
  • Gentle particle motion to minimize agglomeration
  • Suitable for pilot and production scale pharmaceutical processing
  • Improved product recovery and batch reproducibility

Configuration and quotation

To specify the correct pharmaceutical filter dryer, the following parameters are typically required:
  • Required screen opening
  • Material of construction
  • Batch capacity
  • Product particle size distribution
  • Slurry composition
  • Required washing stages
  • Required drying conditions
  • Process temperature and pressure
  • Cleaning and sterilization requirements
  • Installation environment and regulatory requirements

Other pharmaceutical aseptic separator sizes

This production scale filter dryer is part of a pharmaceutical aseptic separator series designed for different batch capacities.

These systems allow pharmaceutical filtration processes to be scaled from laboratory development through pilot testing to full production manufacturing.

Technical support and validation

Selecting the correct filtration solution often requires verification under real process conditions. Filtra International supports this process through several practical testing and validation options.

Filter samples – available for compatibility and performance checks in existing filter housings.
Full-scale filter housing rental – for temporary installations or process evaluation.
Laboratory and pilot-scale filtration units – enabling controlled testing before full implementation.
Application testing by our team – customers may send product samples for filtration trials and performance evaluation.

These options allow process validation before committing to a permanent installation.

Not sure if this configuration is right for your application?

Request technical advice

Share a few details about your process and our team can assist with product selection and sizing.

Typical parameters include:

• Flow rate
• Particle size or filtration rating
• Temperature and pressure
• Chemical composition of the media