Decisions with context
Prescribing, clinical data, calculations, rules, alerts and pharmaceutical validation remain connected, so decisions are not separated from the information that supports them.
A clinical and operational platform for customised parenteral nutrition and commercially manufactured bags — connecting prescribing, pharmaceutical validation, preparation, quality control, release and administration in one traceable pathway.
Between deciding on a composition and administering it lie validation, calculations, materials, batches, preparation, controls, documents and handovers between teams. When each stage lives in isolation, context is lost. Parenteris was designed to keep that clinical and operational thread continuous.
Prescribing, clinical data, calculations, rules, alerts and pharmaceutical validation remain connected, so decisions are not separated from the information that supports them.
Materials, batches, instructions, preparation, checks and control remain associated with the same preparation and with the prescription from which it originated.
Release, documents, labels, transport, receipt and administration remain part of the same history, with auditable states and events throughout the pathway.
Parenteris turns this sequence into a coherent digital pathway: it follows prescribing, supports pharmaceutical validation and calculations, organises production and control, and preserves the information required through release and administration.
Clinical data, composition, route and prescribing context.
Pharmaceutical review, calculations, alerts and auditable decisions.
Materials, batches, instructions and independent double checks.
Quality control, microbiology and process evidence.
Release criteria, documentation and final traceability.
Receipt, identification and operational information for safe administration.
From commercial bag selection to additions and release: clinical and operational information linked to the prescription while keeping the preparation traceable.
A composition tailored to the patient, with calculations and validation linked to the preparation pathway.
Commercial presentations with composition review and contextual selection of additions.
Presentations, volume, energy, macronutrients, electrolytes and bag properties, linked to available reference information.
Selection of additions constrained by the presentations, limitations and information documented in the Summary of Product Characteristics.
Resulting composition, osmolarity, administration route, alerts and rationale to support prescribing decisions and pharmacist review.
Identification of batches and additions, preparation where applicable, quality control, release, transport and receipt.
Module status: Under development and testing in RC2/UAT. This presentation does not imply validation of every bag, clinical authorisation or availability for production use.
Explore the commercial bag moduleClinical logic remains within Parenteris. External integrations use defined contracts, explicit permissions and minimised data.
The pathway is shared, but responsibilities are not. The interface follows that separation.
Prescribing, clinical data, decisions and therapeutic continuity.
Pharmaceutical validation, clinical oversight, release and pathway governance.
Preparation, materials, production, QC and traceability.
Receipt, identification and information required for administration.
Request a demonstration, send an institutional enquiry or register your interest in the brochure. This form does not store these data in the Parenteris clinical database and must not be used to send identifiable patient data, real prescriptions or other confidential clinical information.
Discover a platform designed to keep clinical information, validation, production, control and traceability connected throughout the entire pathway.