Augmenticon ONE

From order to patient.
One platform for radiopharmacy.

Manufacturers, hospital radiopharmacies and nuclear medicine departments work in one system: orders, production, quality control and administration, with one audit trail.

The platform

One platform. Three products. Six systems replaced.

Each product combines two systems that are usually bought, validated and connected separately.

PLAN

Orders, production planning & inventory

OMSMRP
MAKE

Production records & quality control

MESLIMS
CARE

Hot lab & patient dose

HLMSPDMS
CARE → PLAN · clinics order from manufacturers
QMS · powered by Qualio
Documents, training, deviations & CAPA, change control, suppliers
Augmenticon ONE coreSHARED BY EVERY PRODUCT
  • Roles & sites
  • Audit trail
  • E-signature
  • Workflow engine
  • Master data
INTERFACES HL7 / DICOMDose calibrator & QC instrumentsERP / financeOpen API
OMS
Order Management System
MRP
Manufacturing Resource Planning
MES
Manufacturing Execution System
LIMS
Laboratory Information Management System
HLMS
Hot Lab Management System
PDMS
Patient Dose Management System
Products

What each product does today, and what comes next.

AVAILABLE
In the product and in use today
PILOT
Running in a pilot at a customer site
IN DEVELOPMENT
Being built now, demo possible
CO-DESIGN
Being designed now in workshops with customers
PLANNED
On the roadmap

PLAN

OMSMRP

Orders flow straight into production.

1 AVAILABLE · 2 IN DEVELOPMENT · 1 CO-DESIGN · 3 PLANNED
  • Batch planning and assignmentAVAILABLE
  • Inventory with stock levels, low-level and expiry warningsIN DEVELOPMENT
  • Transfers between sitesIN DEVELOPMENT
  • Customer portal for clinics, distributors and study sitesCO-DESIGN
  • Production calendars and capacity based on required activityPLANNED
  • Order deadlines, cancellations and release documents shared with the customerPLANNED
  • Manufacturing status visible to the customer in real timePLANNED

MAKE

MESLIMS

Production records and quality control you can defend.

8 AVAILABLE · 2 PILOT · 3 CO-DESIGN · 1 PLANNED
  • Typed steps with limits, checked at entry Details →AVAILABLE
  • Corrections only with a reason; nothing is deleted (append-only)AVAILABLE
  • Electronic signatures with re-authentication, two or more signers Details →AVAILABLE
  • Training linked to each master record versionAVAILABLE
  • Material receipt with quarantine and release; supplier managementAVAILABLE
  • Equipment with qualification, maintenance and calibration due datesAVAILABLE
  • Computer-vision step control also standalone as Pocket → Details →PILOT
  • Samples, specifications and test plans per productCO-DESIGN
  • QC instrument integration (radio-HPLC, TLC scanner, dose calibrator)CO-DESIGN
  • OOS handling, stability and CoA generated from raw dataCO-DESIGN
  • Paper procedures turned into digital record drafts through guided questions Details →PILOT
  • Report import: report contents mapped once into batch record fields, then reused Details →AVAILABLE
  • Recorded sessions kept with the work record for critical steps Details →AVAILABLE
  • Ask your data: questions about authorized production records, with your own AI Details →PLANNED
Explore MAKE →

CARE

HLMSPDMS

Nuclear medicine, from patient list to PACS.

4 AVAILABLE · 1 IN DEVELOPMENT · 1 CO-DESIGN
  • HOT LAB
  • Daily planning of examinations and tracer demandAVAILABLE
  • Kit preparation with generator eluates (e.g. Tc-99m, Ga-68)AVAILABLE
  • Dose dispensing and measurement incl. residual activity of the empty syringeAVAILABLE
  • PATIENT
  • Administration record and medical eventsAVAILABLE
  • DICOM export of the administered dose, incl. exam ID from the RISIN DEVELOPMENT
  • Ordering of non-produced tracers directly from manufacturers via PLANCO-DESIGN

QMS

Quality management, integrated.

1 AVAILABLE · 1 PLANNED
  • Document control, training, deviations & CAPA, change control, supplier qualification by QualioAVAILABLE · VIA QUALIO
  • Deviations and OOS flow into QualioPLANNED
Ask your dataPLANNED

Ask your AI about your production.

Planned: use the AI you already work with on your Augmenticon ONE records. It will ask as the signed-in person, see only what that person may see, and not be able to change anything. Every call will be logged.

  • Investigate a batch“What differs between this batch and the last ten successful batches?”
  • Understand a trend“Our yield has been declining. What changed over the same period?”
  • Review performance“How did production last week compare with the same period last year?”
Augmenticon PocketPILOT

One check before the run. On a phone.

Pocket is the computer-vision check from MAKE, on its own. Photograph the mounted synthesis cassette; a model on the phone checks syringes, vials, cassette locks and orientation, and hands everything it cannot read to a person to confirm. Nothing to install in your systems, nothing else to change.

Now in a pilot with one of the largest radiopharmaceutical networks, on one of the most widely used products in the field.

  • Photos are read by a model on the phone itself.
  • What cannot be read is flagged, not guessed: a person confirms each point.
  • Works alone, or as one step inside a MAKE production record.
Try the demo app (opens in a new tab) Add it to your phone’s home screen and walk through the examples. No account needed.
More about Pocket →
How it connects

One record from order to administration.

  1. PLAN
    01

    A clinic orders a tracer for tomorrow’s patients.

  2. PLAN
    02

    The manufacturer’s batch plan updates automatically.

  3. MAKE
    03

    QC results and release documents are attached to the batch.

  4. CARE
    04

    The hot lab receives the dose and its documents.

  5. CARE
    05

    The administered dose goes to PACS as a DICOM object.

    IN DEVELOPMENT

One record from the site’s order to drug accountability.

  1. CLINICAL SITEPLAN
    01

    The site orders study medication for its next patients.

  2. MANUFACTURERMAKE
    02

    The contract manufacturer makes and releases the batch; the record stays visible to the sponsor.

  3. LOGISTICS
    03

    The shipment leaves with its release documents and temperature logger.

  4. CLINICAL SITECARE
    04

    The site confirms receipt in the same record, and the temperature data come back with it.

    The handover that usually breaks.
    PLANNED
  5. CLINICAL SITECARE
    05

    The administration is recorded, and drug accountability is complete without re-typing.

    Hand-off to eCRF / accountability log PLANNED
Shape it with us

We build the next features with our customers.

The PLAN customer portal, the QC extensions in MAKE and the next CARE features are being shaped right now in workshops with users. If you run a radiopharmacy or a nuclear medicine department, your requirements can still become part of the product.

Join a workshop