Industry
MES for light pharmaceutical production
Light pharmaceutical and parapharmaceutical sites structure demanding batches, quality checks and production histories. A MES platform supports operational traceability and quality data centralization for production performance and internal reviews.
Challenges
Industry challenges
- Build a clear production history by batch and period.
- Centralize quality checks and their results per batch.
- Monitor downtime and its impact on batch consistency.
- Prepare production data useful for internal reviews.
- Reduce manual file reconstruction effort.
Shop floor problems
What slows production execution today
- Production history scattered across multiple systems and Excel files.
- Quality checks documented on paper then re-entered later.
- Downtime noted late, without precise context.
- Internal documentation preparation is time-consuming.
- No consolidated view of the actual production of batches.
What IBRIXIO delivers
How IBRIXIO responds
- Structured batch traceability and production history.
- Quality checks documented and tied to batches and machines.
- Downtime qualified at the source and usable in reports.
- Regular production reports, ready to share internally.
- Reliable shop floor data to support operational steering.
Indicators
What you monitor
Tracked indicators :Traced batchesOK/NOK quality checksQualified downtime durationProduction history coverageGenerated production reportsFile preparation time
Use case
On the shop floor
To prepare an internal review, the production team consults a campaign history in the platform: batches, machines, periods, qualified stops and related quality checks.
Ready to make your production data reliable?
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