Lab scale pharmaceutical filter dryer for aseptic filtration and vacuum drying of pharmaceutical solids

Lab Scale Pharmaceutical Filter Dryer for Aseptic Filtration and Vacuum Drying (1 kg Batch)

20 µm / 300 mm chamber diameter
€0,00
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Lab scale pharmaceutical filter dryer for aseptic filtration and vacuum drying of pharmaceutical solids

Lab Scale Pharmaceutical Filter Dryer for Aseptic Filtration and Vacuum Drying (1 kg Batch)

Micron Rating
Dimensions

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Product description

A lab scale pharmaceutical filter dryer is an aseptic processing system designed for batch filtration, washing, dewatering, and vacuum drying of pharmaceutical solids within a sealed environment. The system integrates multiple processing stages into a single closed chamber to maintain sterility and minimize product handling. This type of equipment is commonly used in pharmaceutical laboratories and research environments where precise process control, contamination prevention, and reliable batch reproducibility are required.

Technical overview

The lab scale pharmaceutical filter dryer combines vibratory filtration with vacuum drying technology to process pharmaceutical slurries in a compact laboratory-scale unit. The system allows liquid-solid separation to occur on a screening surface while retaining the product solids inside the chamber. Following filtration, the retained solids can be washed and dewatered on the screen. The same chamber is then used for controlled vacuum drying. The design allows laboratory teams to perform multiple processing steps without transferring material between separate pieces of equipment. The equipment is typically used for process development, laboratory-scale manufacturing, and scale-up studies for pharmaceutical filtration and drying operations. :contentReference[oaicite:0]{index=0}

Operating principle

The separator uses vibratory motion to promote efficient liquid-solid separation at relatively low differential pressure across the screen surface. Slurry enters the chamber and spreads across the screening deck. Liquid passes through the screen openings while the solids remain on the surface. The vibratory motion keeps the particles moving across the screen, promoting efficient drainage and reducing screen fouling. After the filtration and optional washing stages, vacuum drying is initiated within the sealed chamber. Controlled gas flow, typically nitrogen, is introduced beneath the product bed to remove moisture while maintaining gentle movement of the solids. This vibratory motion distributes the particles across the screen and improves drying efficiency while reducing agglomeration of fine powders. :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.

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 particle size cut point during filtration and influences filtration rate and product retention.

Design and construction

The filter dryer is constructed as a compact sealed processing unit designed for sterile pharmaceutical processing. Typical design features include:
  • Sealed pressure vessel process chamber
  • Vibratory screening surface
  • Integrated filtration, washing, and drying stages
  • Vacuum drying capability
  • Controlled gas purge for moisture removal
  • Crevice-free hygienic internal surfaces
  • Clean-in-place (CIP) and sterilization capability
  • Sealed product discharge
  • Batch processing configuration
The sealed design minimizes contamination risks and allows safe handling of highly potent pharmaceutical compounds.

Typical applications

Typical applications include:
  • Active pharmaceutical ingredient (API) filtration
  • Pharmaceutical slurry filtration
  • Laboratory filter drying
  • Crystallization process filtration
  • Fine chemical separation
  • Biopharmaceutical process development
  • Pharmaceutical R&D processing
  • High-purity compound processing

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 pharmaceutical materials
  • Gentle drying with reduced particle agglomeration
  • Efficient moisture removal during vacuum drying
  • Compact laboratory-scale design
  • Suitable for process development and scale-up studies

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 steps
  • Required drying conditions
  • Process temperature and pressure
  • Cleaning and sterilization requirements
  • Installation environment and regulatory requirements

Other pharmaceutical aseptic separator sizes

This laboratory filter dryer is part of a pharmaceutical aseptic separator series designed for different processing capacities.

These systems allow pharmaceutical processes to be scaled from laboratory development to pilot and 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?

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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