New Tool Development
Controlled drawing and CAD, material, quantities, target service life and sample acceptance requirements.
Review this project →Design for manufacturability, mold and die manufacture, trials and maintenance planning based on the approved part definition.
Select the project type and provide the available records. Existing tools, repairs and transfers require assessment before scope and feasibility are confirmed.
Controlled drawing and CAD, material, quantities, target service life and sample acceptance requirements.
Review this project →Tool identification, available drawings and records, condition, machine interfaces and the proposed transfer scope.
Review this project →Affected features, condition evidence, shot and repair history, proposed revision and required revalidation.
Review this project →Agree the operations, records and approval responsibilities required for the project. Trial count and release timing depend on the results and acceptance scope.
Input: controlled part definition, material, quantities and acceptance targets.
Record the project scope, required information and open decisions.
Review geometry, tool concept, cavities, inserts and process interfaces.
Approve required decisions and the drawing revision before manufacture.
Work to the approved tool design and agreed material requirements.
Inspect and record the tool identification, revision and agreed manufacturing checks.
Run the tool with the selected material, machine and trial conditions.
Record sample results, process observations, corrective actions and revalidation needs.
Review required inspection results and outstanding actions.
Document approval status and the agreed production-release decision.
Track condition, maintenance, repairs, insert changes and revisions.
Agree repair scope, cost and renewed verification when requirements change.
Tooling design begins with the approved part drawing and CAD model, selected material and process, production quantities, target service life and sample acceptance requirements. These inputs define the mold or die concept and the work required before production release.
The design for manufacturability (DFM) review addresses parting lines, draft, shrinkage allowances, wall and rib transitions, cores, slides, shutoffs, gates, runners, venting, cooling and ejection. Trimming, machining allowances, replaceable inserts, cosmetic surfaces and maintenance access are included where applicable to the selected process.
The review records recommended geometry changes, the proposed tool concept, unresolved risks, customer decisions and the drawing revision approved for manufacture. Filling or mold-flow analysis may support this work when its inputs and scope are agreed. Trials are still required to assess the tool with the selected material, machine and production conditions.
Trial records should identify the tool and part revisions, material, sample quantities, inspection results, outstanding actions and approval status. The project agreement defines the required records and responsibilities.
Drawing and tool revisions, resolved DFM decisions, approved concept and any outstanding items.
Material, machine and process conditions; sample quantities, dimensional results and process observations.
Issue list, required changes, responsible parties, revised documents and agreed repeat checks.
Sample approval status, required inspection records, remaining actions and the agreed release authority.
Set the required records, ownership, care and change procedures in the project agreement. Confirm service-life targets and any warranty against the agreed operating and acceptance conditions.
Define design, manufacture, trials, sample quantities and the records included in the quoted scope.
Assess work, responsibility and validation; agree a separate scope or applicable contractual coverage before proceeding.
Agree packing, transport, interface work, recommissioning and documentation responsibilities.
Part size, cavity count, side actions, deep or delicate features, tool material and heat treatment, cooling design, interchangeable inserts, trimming and validation affect tooling cost. Useful service life also depends on operating conditions, maintenance and the dimensional or appearance criteria for continued use.
Before order placement, agree the quotation scope, tool ownership, storage, maintenance responsibilities, spare inserts, approval of changes and the treatment of major repairs or replacement.
Provide the approved drawing and CAD revision, material and process, production quantities, critical features, cosmetic areas, secondary operations and sample acceptance requirements.
Define the design and manufacturing scope, trials, sample inspection, tool ownership, storage, maintenance responsibilities, spare inserts and approval process for changes.
Approval is based on the agreed trial results, sample inspection, resolved corrective actions and required customer authorization. The tool and part revisions must be recorded.
Initial trial results identify sample performance and outstanding actions. The project agreement defines corrective work, further trials, sample approval and production-release responsibilities.
Review the tool condition, documentation, machine interfaces and required acceptance criteria first. Agree any interface changes, repairs and recommissioning before confirming the transfer scope.
Assess the cause and affected features, then agree the work, responsibility, cost and verification requirements before proceeding. Record tool and part revisions and update the applicable approvals.
A practical view of tooling development from requirement review and mold concept through steel release, T1 sampling, correction, approval, and maintenance planning.
Read engineering guide →A drawing-based checklist for closing geometry, tooling, machining, finishing, inspection, and approval questions before die manufacture begins.
Read engineering guide →A practical guide to tooling, material, geometry, process, machining, finishing, inspection, assembly, and change risks that shape total die casting cost.
Read engineering guide →Send the part definition and available tool records so engineering can clarify scope, required decisions and next steps.
Provide the controlled 3D model and drawing, material specification, batch and annual quantities, critical datums, cosmetic areas, secondary operations, target tool life, sample requirements and requested delivery schedule.