Daijyo V · Updated 11 October 2026
Feasibility, validation and shelf-life testing
These answer different questions. Feasibility explores whether the product and packaging make HPP worth pursuing. Process validation establishes evidence for a defined treatment objective. Shelf-life work assesses the finished product over its intended storage period.
Campden BRI describes HPP challenge testing as a specialist investigation using a target microorganism. This work belongs with appropriately equipped specialists, with the study designed around the product and safety objective.
Evidence: Campden BRI: high pressure process challenge testing.
What to bring to the first discussion
- Product type, recipe outline and current process.
- Packaging material, pack size and approximate production volumes.
- Current and target shelf life, with storage and distribution details.
- The safety, quality or commercial question you need answered.
- Any existing laboratory reports or supplier quotations available for a later technical review.
How Daijyo V helps
We help scope the project, identify processing and laboratory support, compare proposals and interpret the commercial implications with you. Trials, laboratory work and processing are delivered by appropriate providers and scoped separately.
How much do HPP trials and processing cost?
There is no single quote that fits every project. A useful request separates sample preparation, processor time, packaging, transport, laboratory work and consultancy. Commercial processing also needs a view of volumes, frequency and logistics.
We help build that comparison so you can decide whether to pursue outsourced processing, equipment investment or another route. Start with a brief outline; you do not need a finished technical specification.