Migrating from a legacy PLM, ERP, ingredient marketplace, compliance tool, spreadsheets, or another export?
Send usable exports, sample files, or API access. Formuley maps formulas, raw materials, formula lines, suppliers, batches, and documents into a verified sample workspace before a production cutover is scoped.
48 hours begins after we receive usable exports, sample files, or API access. Full rollout timing depends on data quality, documents, permissions, validation, and rollout scope.
Migration proof room
Sample workspace before rollout.
Source exports
Proof report
48-hour proof flow
Your team reviews the structure and cleanup scope before committing to a broader rollout.
Hour 0
Share CSV, XLSX, document lists, or API access from your current system.
Within 24 hours
We map formulas, formula lines, raw materials, suppliers, batches, costs, and document metadata into Formuley fields.
Within 48 hours
Your team sees what moved, what connected, and which cleanup items need review.
Next step
The proof report informs validation, training, permissions, and production cutover planning.
Ingredient continuity
Switching systems should not mean rebuilding how your lab sources raw materials. Formuley maps supplier names, SKUs, pricing context, MOQ, lead time, SDS/COA/spec documents, and formula usage from usable exports or files, then shows what is ready and what needs review before rollout.
Supplier names, preferred sources, SKUs, ordering notes, MOQ, and lead time can be reviewed beside each raw material.
SDS, COA, spec documents, pricing context, and cost fields stay visible as part of the proof scope.
Raw materials can stay connected to formula lines so the team sees where each source is used before rollout.
Source systems
The proof is designed for imperfect real-world data. We do not require a perfect template before showing what can move into Formuley.
Formula codes, ingredient libraries, INCI, CAS, phases, percentages, versions, and custom fields.
Item codes, vendors, batches, costing context, production notes, and operational references.
Raw materials, formulas, formula lines, supplier files, SDS, TDS, COA, PDFs, and mixed export bundles.
Ingredient identifiers, screening notes, compliance context, supplier references, and review data.
Records in scope
Records found, records created, skipped rows, duplicates, and formula total checks are visible before rollout.
Unmapped columns, unresolved raw materials, duplicate ingredients, and attachment gaps are called out for review.
The report gives a practical path for validation, training, permissions, and production cutover timing.
Enterprise rollout
Pilot availability, migration support, validation, training, permissions, and commercial terms are handled through your enterprise agreement.
