1. Pharmaceuticals QMS
  2. Integrations
Reference

Integrations

Decide where batch, laboratory and document evidence originates before connecting quality work.

  • Pharmaceuticals QMS
  • Manufacturing or inventory records
  • Laboratory results
  • Environmental monitoring source
  • Document source

Systems to connect

  • Manufacturing or inventory records. Bring the batch or subject identifier into the inspection reference so the quality team can find the originating operation.
  • Laboratory results. Bring the test name, observed value, specification and source evidence into an out of specification case under the right inspection.
  • Environmental monitoring source. Bring the room measurement, unit, action limit and source identity into the linked sample capture.
  • Document source. Attach the approved procedure version to Controlled Documents and retain its effective date.

How connections are governed

Choose one source for each identifier and measurement. Resolve People identities before a person submits a case or sample. Reject an invalid operational inspection link rather than filing a result under an unrelated subject. Keep the source evidence with the submitted context so reviewers can investigate a later correction or a new measurement. Review the data model and implementation phases together.

Set up Pharmaceuticals QMS your way.

Start free, then use Proto to change fields, steps and approvals before your team goes live.

How to get started