Connect formulation, raw materials, production, testing, and customer specifications. Know which lot meets which requirement—and why.
Free forever sandbox · choose a template or build your ownLOT-2408A test result does not automatically qualify a lot for every customer.
For specialty chemical, formulation, and quality teams
Explore the dashboard, open a record, run a step, or resolve a blocked review. Changes stay inside this sample workspace.
Wilmington · Plant 1 · your operation at a glance
A material can have several grades, uses, and customer requirements. Helix connects the lot and its results to the exact specification under review, so a familiar product name does not become a substitute for a release decision.
Shared identities, effective revisions, and review rules connect each team’s work to the next decision.
Compare trial conditions and structured results. Promote the selected formulation through a transfer review that retains its parameter rationale, scale assumptions, and analytical evidence.
Keep ingredients, proportions, instructions, units, and process limits in a versioned formulation record. Review a revision before it governs production.
Track suppliers, grades, lots, receipts, and supporting certificates. Keep the material’s identity separate from the status of a particular lot.
Review reported values with the applicable specification, method, and source evidence. Investigate an exception where the production context is already available.
Link the customer’s approved requirement to the release review and supporting certificate. Keep evidence for the selected grade and use together.
Follow a supplier lot into intermediates, finished lots, and recorded shipments. Keep missing relationships visible as you establish the scope of an investigation.
A generic “passed” label hides the question that matters: passed against what? Carry the exact specification into the decision.
A viscosity result is copied into a certificate.
The release review checks the selected customer specification and the source result before the certificate is approved.
Retain the lot, result, specification revision, and certificate decision together.
An entity definition shapes a record type. Your approved records hold the operating content. Execution captures what actually happened.
Defines the structure and allowed behavior of records of this type.
The CR-42 resin formulation, with its ingredient proportions, mixing instruction, and accepted process range.
A specific record and its effective revisionThe lots charged, actual mixing conditions, samples, results, and disposition for this run.
Actual work linked to its approved sourceA formulation change can affect product specifications, test requirements, and customer commitments. Review those dependencies before the revised formula becomes effective.
Give AI the records and relationships needed to produce a useful draft. Keep the decision with the accountable person.
Explore governed AIHow does this customer’s requirement differ from our current product specification?
A cited comparison of differing limits, units, required evidence, and unanswered questions for technical review.
A person resolves ambiguous requirements and approves the applicable specification.
Keep a clear source of truth for each record. Agree the interfaces, ownership, and exception handling for your deployment.
Connect the customer, product, and order requirement to the appropriate operational records without duplicating financial ownership.
Agree how sample identity, methods, units, results, and attachments enter review. Preserve the distinction between imported data and an approved result.
Bring documents into the material and lot context, with clear verification and approval steps for extracted or entered values.
These are integration boundaries to evaluate, not a list of prebuilt connectors. All plans include unlimited integrations.
Use the application sandbox to choose a template, author your model, and work through the decisions your team makes.
Start with one formulation, two customer specifications, and one lot. Walk through a conforming result and a requirement that needs review.
Extend into supplier qualification, formulation change control, customer-specific release, and connected certificate records.
Start in the free forever sandbox. Explore a template, make it yours, and decide what comes next.