Pharmaceutical calibration operations

Every sensor.
Every site.
One history.

Control temperature and environmental monitoring equipment from deployment and rotation through calibration, technical review and audit evidence.

Explore features

A continuous control loop

Make routine equipment control easier to see and defend

  1. 01

    Locate

    Know which sensor is installed at which client, site and location.

  2. 02

    Plan

    Turn calibration intervals into visible, accountable work.

  3. 03

    Execute

    Follow the applicable controlled procedure and record evidence as work happens.

  4. 04

    Review

    Keep uncertainty, conformity and approval connected to the result.

  5. 05

    Evidence

    Prepare a scoped dossier without reconstructing the history.

Sensor rotation without lost context

Follow equipment between clients, sites and locations

Preserve deployment dates and location history when calibrated sensors replace units in service. Current assignment stays clear while earlier placements remain available for time-scoped evidence.

  • Only unassigned equipment is offered for a new placement
  • Client, site and location context stays attached to each deployment
  • Dossier scope can include every device present during the selected period
Equipment register showing calibration assets and their current deployment context
A practical asset view for equipment that moves through calibration and service.

Controlled work at the point of use

Give technicians the approved method, not another blank form

Versioned procedures guide ordered work and required evidence. Reference standards, uncertainty calculations and conformity decisions remain linked to the calibration event that used them.

See the guided workflow
Technician workspace showing ordered controlled calibration procedure steps
Capture the evidence while the work is being performed.

When results need attention

Keep excursions and follow-through connected

An out-of-tolerance result can open an investigation with impact, containment, root cause, disposition and corrective action linked back to the calibration evidence.

Out-of-tolerance investigation showing impact assessment and corrective action workflow
Keep the quality response beside the result that triggered it.

Evidence ready when review begins

Bring the asset story together.

Prepare site- and period-scoped dossiers from equipment, calibration, certificate, traceability and quality records already captured in Metra.

Audit readiness

Obsidian Metra supports calibration and quality evidence management. It does not provide GMP/GxP validation, confer regulatory compliance, or replace your organisation's validated processes and professional judgement.