DEVELOPMENT & QUALITY
A defined path for reviewing the formula, selecting a suitable BFS format, validating the process and preparing qualified projects for commercial production.
From brief to production readiness.
From brief to production readiness.
View the development path
Request a qualification review
A controlled development path.
A controlled development path.
Each project follows a defined sequence with a clear decision at every stage. The path may be adjusted after technical review.
Project brief
Project brief
Define the formula, target dose, intended use and launch requirements.
Formula review
Formula review
Review composition, stability concerns and process suitability.
Select the BFS format and review formula-pack interaction.
Format & compatibility
Format & compatibility
Pilot validation
Pilot validation
Production readiness
Production readiness
Confirm forming, filling, sealing and performance under production conditions.
Finalize specifications, process parameters and the commercial production plan.
Formula status
Formula status
Viscosity & composition
Viscosity & composition
Fill volume
Fill volume
Package compatibility
Package compatibility
Intended use
Intended use
Target market
Target market
TECHNICAL REVIEW
The first review combines formula needs with how the finished product will be used, presented and produced.
What we review before production.
What we review before production.
Quality is reviewed across the BFS process. The exact checks and retained records depend on the selected project route.
Container geometry and visual consistency.
Dose accuracy against the approved range.
Seal integrity and container closure.
Defined testing according to the project.
Clarity, finish and cosmetic quality.
Final review before handover or shipment.
Records are grouped by purpose and depend on the selected project scope.
PROJECT RECORDS
Approved specifications
Pilot or trial records
Inspection and quality records
SUPPORTING DOCUMENTS, WHERE APPLICABLE
Certificate of Analysis
Safety Data Sheet
Material and compatibility information
Document availability depends on the selected route, materials, manufacturing scope and responsible party.
Manufacturing and quality checkpoints.
Manufacturing and quality checkpoints.
Forming
Forming
Filling
Filling
Sealing
Sealing
Leak check
Leak check
Appearance review
Appearance review
Pack-out release
Pack-out release
Evidence and documentation.
Evidence and documentation.
Prepare your project for review.
Prepare your project for review.
QUALIFICATION REVIEW
Share enough information for the team to assess the likely development route before samples, tooling or pricing.
Formula status and stability concerns
Target dose, volume and preferred format
Intended market and launch timing