Client leads
- Market, brand and commercial direction
- Programme targets and acceptance decisions
- Pilot, production, launch and material-change approvals
Manufacturing · Programme-specific responsibility
Build manufacturing confidence before production begins.
Natural Origin Life connects the approved product brief to programme-specific manufacturing support. The responsible manufacturer, production site and included activities are defined for each product and programme, and confirmed with you before production begins.
Eight stages connect the brief to controlled delivery and change.
The stages organise the work. Client approval gates define when targets, plans, production release, launch and material changes can move forward.
DFM
Review geometry, materials, tolerances, assembly choices and process implications against the agreed brief.
G1 Program brief / targets approved
Sourcing
Define material, component and supplier requirements together with evidence and change-control expectations.
G2 Design + validation plan approved
Tooling
Translate the approved design intent into the tooling and process plan required by the programme.
G2 Design + validation plan approved
Validation
Run the agreed validation plan and keep observations, limitations and approval evidence connected to the configuration reviewed.
G2 Design + validation plan approved
Pilot
Use the pilot to review process readiness, product evidence and unresolved issues before production release.
G3 Pilot + production release approved
QC production
Execute the approved production and inspection scope under product-, programme- and site-specific records.
G3 Pilot + production release approved
Delivery
Connect the approved release state, delivery requirements and programme records before launch.
G4 Launch / material-change approval
Change control
Route an approved material, supplier, process or configuration change through the agreed review before implementation.
G4 Launch / material-change approval
Responsibility remains visible at every stage.
The programme record distinguishes the client decision, Natural Origin Life support, responsible manufacturer, production site and evidence owner for the scope at hand.
Programme backbone records
- Included development and manufacturing support scope
- Responsible manufacturer and production-site mapping
- Validation, inspection, traceability and change records
Review the evidence system behind the programme.
See how quality planning and testing evidence support each approval decision.