COMMERCIAL FREEZE DRYERS FOR BIOTECHNOLOGY & BIOENGINEERING

Scale Freeze-Drying Processes for Biological Materials, Cultures, Proteins and Specialized Ingredients from Development Through Production.

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From biological material to controlled dry format

Build the cycle around the function, structure and recovery that matters.

Freeze drying can help convert sensitive biological formulations into dry, porous formats for storage, handling or later constitution. Performance depends on formulations, freezing behavior, process conditions and packaging.

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Bioengineering Applications Worth Evaluating

The right process starts with the material and its intended use.

Microbial Cultures

Fermentation products, starts cultures and microbial materials where recovery and viability can be measured.

Proteins + Enzymes

Functional proteins, enzymes and peptides where activity, structure and reconstitution must be evaluated.

Boimaterials + Scaffolds

Hydrogels, porous matrices and engineered materials that require controlled structure after drying.

Research Reagents

Assay components, standards and specialty formulations developed for storage or later reconstitution.

Agricultural Biologicals

Microbial inoculants, biological inputs and related formulations where the process and facility are suitable.

Process Development

Pilot work for formulation screening, endpoint definition, analytical testing and commercial scale up.

Product development principle

Start with the function you need to retain then connect formulation, cycle, handling and testing to that requirement.

That is how a promising development result becomes a repeatable production process.

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Sean Jones, Owner, Foodynamics

“Parker was really there as a strategic partner with us right from the beginning. And I don't think there's many companies that provide that level of service or philosophy. And I'm not just saying in the freeze dried industry or as an equipment manufacturer – I’m saying in any industry.”

Freeze Drying is not sterilization

A successful cycle does not establish sterility, activity or shelf life.

Those requirements depend on the full formulation, facility controls, analytical meths, packaging and validation program. Equipment selection must match the materials intended use and regulatory environment.

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