Solution

Central IV Compounding

Reconstitution, filling and batch preparation are brought into a repeatable workflow supported by dedicated equipment and configured components.
Central IV admixture preparation
Customer need

The operational question this solution answers

Centralised IV preparation increases volume and repetition. Manual reconstitution and filling make consistency harder to maintain and place a documentation burden on pharmacy staff.

Key benefits

Practical value in the workflow

Repeatable filling

Defined volumes are delivered consistently across a preparation run.

Supported reconstitution

Dedicated equipment handles dissolution steps within the workflow.

Batch consistency

The same configured route is followed for each unit in a batch.

Project integration

Equipment is specified against the room, volume and product mix in scope.

Differentiators

What KAPSAM brings to this scope

Scoped to real volume

Configuration follows the preparation volumes the pharmacy actually runs.

Component compatibility

Bags, sets and filling components are specified with the equipment.

One support route

Installation, service and consumable supply stay with one responsible party.

Workflow

5-step workflow

  1. 01PlanBatch and product mix are defined.
  2. 02ReconstituteDissolution steps follow the configured method.
  3. 03FillTarget volumes are delivered into the selected containers.
  4. 04CheckPreparation is verified against the batch definition.
  5. 05ReleaseBatch records are completed.
Software and connectivity

Where this workflow meets hospital systems

Workflow software scope for central IV preparation is defined during project assessment and documented here once confirmed.

PharmaScope Software workflow
Evidence

Verified projects and references

Project references are published only with written customer permission. Ask for the references relevant to your application area and country, and we will share what has been approved for release.

Technical overview

Specification and regulatory information

Equipment specification, throughput figures and regulatory status are published here once Product and Quality review is complete.
Resources

Documents and further reading

Datasheets and technical documents for this solution.

Workflow and product overview films.

Background reading on this application area.

Questions

Frequently asked questions

The answers below cover what hospital pharmacy, IT and technical teams ask most often. If your question is not here, our team will answer it directly.

Where does a compounding project start?

From the preparation you need to improve rather than a product list: application area, daily preparation volume and the hospital systems already in place define the scope.

Is the scope limited to equipment?

No. Automation, workflow software, HIS/EHR connectivity, sterile disposables and the controlled environment are specified together, so responsibility is not split across suppliers.

How is each preparation documented?

Order entry, clinical review, preparation and verification steps are captured as traceability records, which can be reported for quality and audit purposes.

Discuss this workflow with our team

Tell us about your preparation volume, application area and hospital systems. We will respond with the relevant technical and project information.