Solution

Parenteral Nutrition Compounding

Automated compounding, workflow software and configured sterile disposables are planned together, so patient-specific PN preparation follows one defined and verifiable route.
Parenteral nutrition compounding workflow
Customer need

The operational question this solution answers

Patient-specific parenteral nutrition depends on accurate calculation, correct ingredient access and repeatable preparation. When ordering, review and preparation live in separate systems, verification effort rises and the workflow becomes harder to evidence.

Key benefits

Practical value in the workflow

Gravimetric verification

Each addition is checked by weight during preparation rather than after the fact.

Configured fluid paths

Ingredient access is set up around the formulas the pharmacy actually prepares.

Connected order entry

NutriSoft carries the order and calculation into the device workflow.

Recorded preparation

Each preparation produces records that support review and reporting.

Differentiators

What KAPSAM brings to this scope

One project conversation

Device, software and disposables are scoped together rather than procured separately.

Connectivity assessed early

HIS/EHR boundaries and data exchange are reviewed before commitment.

Supported lifecycle

Installation, training, technical service and consumable supply run from one responsibility.

Workflow

5-step workflow

  1. 01OrderPatient and formula data enter the workflow.
  2. 02ReviewClinical rules and calculation are applied.
  3. 03PrepareAutomated compounding follows the configured fluid path.
  4. 04VerifyGravimetric control confirms each addition.
  5. 05ReleaseRecords are completed and the preparation is released.
Software and connectivity

Where this workflow meets hospital systems

NutriSoft supports order entry, calculation and workflow control for PN preparation, and is the point where hospital system integration is assessed.

NutriSoft interface
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

Technical specification, configuration options, installation requirements 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.