PRISTINE DENTAL DESIGN — FULL-ARCH HANDOFF & REVIEW CHECKLIST
Prepared October 6, 2026. Operational aid, not a clinical protocol.
Use internal identifiers. Keep case records in the agreed controlled transfer route.

BEFORE SETUP
[ ] Arch, indication and intended provisional / final stage identified
[ ] Current clinician-approved plan and prescription supplied
[ ] Working/opposing records and approved bite identified
[ ] Tissue/reference/provisional records identified where relevant
[ ] Approved reference version distinguished from unapproved proposals
[ ] Physical components and digital library/version confirmed where applicable
[ ] Missing or conflicting information documented with a decision owner

SETUP REVIEW
[ ] Reviewer and design version recorded
[ ] Views/references used for review recorded
[ ] Approved elements listed explicitly
[ ] Requested changes consolidated by unit/arch and view
[ ] Unresolved requirements and next milestone recorded
[ ] Setup approval distinguished from manufacturing release

PRODUCTION HANDOFF
[ ] Supported material and manufacturing route confirmed by receiving lab
[ ] Required output formats and separate files identified
[ ] Applicable component/material requirements checked by responsible team
[ ] Receiving workflow import and intended file relationships checked
[ ] Approved output version recorded
[ ] Clinical and manufacturing approval responsibilities identified

CHANGED INPUTS
[ ] Replacement records identify which prior version they supersede
[ ] Affected design decisions / outputs identified for review
[ ] Scope, target and review milestones reconsidered where necessary

CAD views do not establish clinical fit, passive fit or patient outcomes.
The checklist does not supply universal geometry or manufacturing settings.