Complidara

Dietary supplement incoming quality.

Part 111-style evidence. Receiving AI suggests HOLD or RELEASE with citations. QC confirms. Nothing auto-releases.

app.complidara.com
COASPECLot VC-26099Assay 99.4%Identity FTIRLead 0.82 ppmArsenic 0.04 ppmSupplier PDF — citedAssay min 99%passIdentity presentpassLead max 0.5 ppmfailSUGGESTIONHOLD
Deterministic min/max compare. The model is not asked whether the lot is compliant.

How it works

From PDF to a documented suggestion.

  1. 01

    Intake

    Bring a supplier CoA into Evidence or CoA intake.

  2. 02

    Compare spec

    Receiving AI extracts tests and compares them to your active spec.

  3. 03

    QC confirm

    Reviewer or admin records HOLD, RELEASE, or REJECT. Override needs a note.

  4. 04

    Brief

    Generate a brief or audit-prep pack from the live register.

Suites

Named areas in one product.

Core

  • Dashboard posture (certs, findings, lots waiting on QC)
  • Ask Complidara — cited Part 111-style answers
  • Control packs
  • Ingredient specs (min/max limits)
  • Suppliers
  • Evidence inbox
  • Assessments
  • Findings
  • Briefs
  • Audit-prep packs

Incoming Quality

  • QC queue
  • Today’s incoming worklist
  • CoA intake
  • Certificate monitor (expiry / mismatch → findings)
  • Supplier questionnaires
  • Receiving AI — CoA vs spec; HOLD / RELEASE / REJECT / NEEDS_REVIEW suggestion

Receiving AI

A named module inside Incoming Quality. Lot + CoA + spec → suggestion. Confirm RELEASE does not post to your ERP.

SUGGESTIONHOLDNOT A RELEASEQUALITY CONTROLConfirmsNamed user + timestampNOTHING AUTO-RELEASES

Plant Operations is quoted separately. Pricing

What it will not do

No overclaim.

  • Not FDA approved. Not a guarantee of compliance.
  • Does not replace QC judgment or identity testing required by Part 111.
  • Does not auto-release a lot. Ask Complidara does not confirm RELEASE.
  • Not a medical product. Not Complidara Market — that is a separate line.