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EquatorOps

Regulated operations

Make quality part of the way the work gets done.

Connect receiving, inventory, and release to the procedures, inspections, training, and evidence that govern them. Give warehouse, manufacturing, and quality teams a common operational record.

Operations / inventory workspaceInspect screen
Actual EquatorOps warehouse locations showing receiving and shipping staging, dock doors, quarantine and damage areas
Captured from the running app · anonymized demonstration records
Operations / inventory workspace

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Actual EquatorOps warehouse locations showing receiving and shipping staging, dock doors, quarantine and damage areas

01 / Connect movement to control

From receipt to release, carry the quality context.

A stock position tells you what is present. The operational record also needs to explain where it came from, which lot it belongs to, whether it is held, and what supports its release.

RECEIVING → CONTROLLED STOCK → RELEASEIllustrative workflow
  1. 01 / RECEIVEIdentify the stock

    Item, lot, handling unit, and receipt context

  2. 02 / INSPECTRecord the outcome

    Checks, observations, and linked evidence

  3. 03 / CONTROLHold or disposition

    Keep affected inventory from moving through release

  4. 04 / RELEASEReview readiness

    Authorized action with its supporting record

ONE CONNECTED RECORD

Custody · location · quality state · decisions · evidence

A control model for a configured workflow. Applicable checks and release responsibilities depend on the operation.

02 / Run the operation

Inventory context that survives the handoff.

Lots & handling units

Track lot and expiry context alongside stock and nested LPNs. Preserve the relationship between items, cases, pallets, locations, and their movement records.

Holds & release gates

Place quality holds on affected inventory and enforce the applicable movement and release restrictions. Keep the hold reason, disposition, and release evidence together.

Work & inspections

Connect receiving and execution to inspection outcomes and exceptions. Give operators and quality reviewers the same record to follow through the next step.

Custody & traceability

Follow inventory through location changes and transfers. Use the transaction history to investigate what happened to the stock and the work around it.

03 / Operate the quality system

GMP work is a daily operating rhythm.

For medical device warehouses, 3PLs, and manufacturing teams, audit preparation depends on procedures being followed over time. Connect the procedure revision, the people trained on it, the checks performed, and the response when a result falls outside expectations.

CONTROLLED PROCEDURES

The current instruction

Release documents, manage revisions, and schedule periodic review.

TRAINING & ROUTINE CHECKS

The work in practice

Connect each role to required training, completion, and competence checks. Capture scheduled facility and operational checks.

NONCONFORMANCE & CAPA

The response to a gap

Assign corrective work and retain evidence of follow-through.

Explore the connected quality system

04 / Prepare for the next review

Build the evidence while the work happens.

Audits & findings

Run guided audits, capture observations, assign findings, and track remediation. Keep owners, due dates, and closure evidence in the quality record.

Reviewable evidence packages

Assemble linked records and supporting evidence for internal reviews, customer requests, and audit responses. Retain the history behind the package.

Configure the system around your procedures and assessment requirements. Software supplies the workflow and records; your organization owns the operating practices and evidence of their effectiveness.

Connect suppliers & operating partners

Start on the floor

Choose one receipt, one hold, or one audit finding.

We’ll follow it through your operation and map the records, responsibilities, and quality gates that need to stay connected.

Request an operations walkthrough