Plug'n'Dose

Therapeutic drug monitoring · MIPD

The right dose, for the right patient, at the right time.

Plug'n'Dose distributes, integrates and supports Tucuxi, decision support software developed by CHUV and HEIG-VD. Using population pharmacokinetic models and Bayesian inference, Tucuxi helps personalise dose adjustment.

  • Developed since 2012 by CHUV and HEIG-VD
  • Open source
  • Already in use in several university hospitals
From population model to patient
Demonstration · fictitious drug
  • Predicted median
  • 25th to 75th percentiles
  • 5th to 95th percentiles
  • Trough target
  • Dose
  • Measurement
  • Without adjustment
Measured concentration
17.0mg/L Sampled at 35.5 h, before the 4th dose
Estimated clearance
3.2L/h 90% interval: 2.7 to 3.8 L/h
Steady-state trough
18.1mg/L Above target Current dosage, target 8 to 15 mg/L
Suggested dosage
750mg every 12 h Predicted trough: 13.6 mg/L, from the 5th dose
Drag the measurement to recalculate the prediction

Illustration with a fictitious drug and a simplified model. Try the real Tucuxi calculation engine

Plug'n'Dose

Making therapeutic drug monitoring simpler and more accessible

A French company founded in 2025, we make Tucuxi installable, connected to your systems and used day to day.

A clinical, technical and operational alliance

  • Julien Massari

    Founder and President

    Pharmacokinetics engineer.

  • Prof. Thierry Buclin

    Scientific and clinical lead

    Pharmacologist, professor emeritus at CHUV, initiator of Tucuxi.

  • Prof. Yann Thoma

    Technical lead

    Professor at HEIG-VD, lead developer of Tucuxi.

How it works

From a measurement to a personalised dosage

  1. Data

    Automatic retrieval

    The assay result and the patient context (identity, dosage, dosing times, weight, age, creatinine) are retrieved from the health record or the laboratory system. No manual re-entry, fewer identification errors.

  2. Model

    Population model

    Each drug is described by a drug model file: a published population pharmacokinetic model, its covariates, its therapeutic targets and the available doses.

  3. Computation

    Bayesian inference

    The computation engine confronts the model with the patient's measurement. The broad population distribution narrows into an individual a posteriori estimate, with its uncertainty.

  4. Recommendation

    Personalised dosage

    Tucuxi assesses the current dosage against the target, suggests an adjustment and predicts its effect. The interpretation report is ready to send; the decision remains with the prescriber.

Demonstrator

The Tucuxi engine, in your browser

A fictitious patient, five public drug models and the actual Tucuxi computation engine. Change a value: the prediction and the suggested dosages are recalculated.

The demonstrator requires JavaScript and WebAssembly. For a guided demonstration, contact us.

Local computation by tucuxi-core (HEIG-VD and CHUV, AGPL v3 licence, sources), drug models from the public tucuxi-drugs repository. Nothing is sent to a server. This demonstrator is not CE marked and must never be used to determine a patient's dosage.

Why a model

Each patient has their own pharmacokinetics. And their own dosage.

Therapeutic drug monitoring (TDM) measures a drug's concentration to adjust each patient's dose.

Keeping exposure within the therapeutic window: neither underdosing nor overdosing.

Empirical TDM

A measurement, a rule

  • Assumes steady state
  • Requires precise sampling times
  • Adjusts the dose by simple proportion

MIPD

A measurement, within a model

  • Uses every measurement, even before steady state
  • Accounts for the patient: weight, age, renal function
  • Predicts the effect of the adjustment

Tucuxi

Open software, from public research

Developed at CHUV and HEIG-VD, published as open source, with its drug models publicly available.

Already in use in several university hospitals

  • CHUV
  • AP-HP
  • AP-HM
  • HCL

Open-source version, at the institutions' own initiative.

An evaluated and published technology

Piperacillin: target attainment by dosing strategy

Estimated probability of reaching the target trough (8 to 32 mg/L), 80 treatment courses analysed with Tucuxi

  1. Same dosage for all, 4 g every 8 h32%
  2. Actual initial dosage, from the medical record32%
  3. Empirical TDM, after the 1st assay55%
  4. A priori MIPD, without measurement29%
  5. A posteriori MIPD, after the 1st assay83%
  6. A posteriori MIPD, after 2 assays94%
A posteriori Bayesian adjustment (MIPD)Other strategies
Retrospective scenario analysis. The authors stress that prospective trials are still needed to confirm the benefit on clinical outcomes. Haefliger D. et al., J Antimicrob Chemother, 2025. doi:10.1093/jac/dkaf007

Application areas

  • Anti-infectivesCefepime, daptomycin, darunavir, dolutegravir, doravirine, gentamicin, lopinavir, meropenem, piperacillin, rifampicin, teicoplanin, tobramycin, vancomycin.
  • Oncology and haematologyBusulfan, imatinib, ponatinib, venetoclax.
  • TransplantationTacrolimus.
  • CardiologyApixaban.
  • Inflammatory diseasesBiologics, anti-TNF.Drug model to create for the project
  • Neurology and psychiatryAntiepileptics, lithium, psychotropics.Drug model to create for the project
Especially useful in
  • Intensive care
  • Paediatrics and neonatology
  • Renal or hepatic impairment
  • Obesity
  • Renal replacement therapy
  • Extracorporeal circulation
View the references of the published models
Apixaban
Cirincione
Busulfan
Ben Hassine (adults), Ben Hassine (paediatrics), Paci
Cefepime
Buclin
Daptomycin
Dvorchik
Darunavir
Daskapan
Dolutegravir
Barcelo
Doravirine
Yee
Gentamicin
Fuchs
Imatinib
Gotta
Lopinavir
Fuchs
Meropenem
Li
Piperacillin
Chen, Li
Ponatinib
Hanley
Rifampicin
Svensson
Tacrolimus
Andrews, Cai, Monchaud, Nanga, Sikma, Storset, Han
Teicoplanin
Ogami
Tobramycin
Hennig
Vancomycin
Colin, Dao, De Cock, Frymoyer, Goti, Grimsley, Liu, Llopis-Salvia, Staatz, Thomson, Yamamoto, Kimura, Lee, Lo, Mehrotra, Mulubwa
Venetoclax
Brackman

Catalogue checked on 30 September 2026 against the official list of Tucuxi models. Several models may apply to different populations. The demonstrator above loads five drug models; this catalogue lists all the models published on the official website.

Tucuxi technical sheet
Licence
Open source, AGPL v3
Origin
Clinical pharmacology at CHUV and HEIG-VD, since 2012
Computation
Bayesian inference: population, a priori and a posteriori predictions, percentiles
Targets
Trough, peak, AUC, cumulative AUC, AUC/MIC, time above MIC
Routes
Intravenous bolus, infusion, extravascular route
Connectivity
Reading from and writing to a remote database (LIS, EHR), import of requests in XML
Output
Interpretation report for the prescriber

Regulatory status: open-source version without CE marking, medical device marking planned. Learn more

Accompagnement

A project, in three stages

We take care of what separates open software from a tool used every day in your departments.

  1. 01

    Scope

    Drugs, patients and data flows concerned.

    • Model selection
    • Regulatory process
  2. 02

    Connect and configure

    Connection to your systems, drug models.

    • Distribution
    • LIS and EHR integration
  3. 03

    Train and support

    Hands-on training, then long-term follow-up.

    • Training
    • Maintenance

Start with a conversation

Questions

Frequently asked questions

Another question about Tucuxi or a deployment project? Write to us.

Is a concentration measurement needed to use Tucuxi?

No. Without a measurement, Tucuxi provides an a priori prediction based on the population model and the patient's characteristics. Each measured concentration then refines the a posteriori prediction, including outside steady state.

Does Tucuxi replace the pharmacologist's expertise?

No. Tucuxi is a decision support tool: it computes, positions the measurement and suggests a reasoned adjustment. The decision remains with the prescriber, informed by the opinion of the pharmacologist, pharmacist or laboratory biologist.

Which drugs are available?

The Tucuxi catalogue lists 19 drugs and 43 models (see application areas and models). Five drug models are loaded in the demonstrator. Any drug with a published model can be given a new drug model, created with the online editor; we support model selection and the creation of the drug model.

What is the regulatory status of Tucuxi?

The open-source version of Tucuxi is not a CE-marked medical device: it is used under the responsibility of the institutions that install it. CE marking as medical device software is a Plug'n'Dose project.

Is Tucuxi open-source software?

Yes. It is released as open source under the AGPL v3 licence and its drug models are in a public repository. Plug'n'Dose provides installation, integration with information systems, training and the regulatory process.

Contact

Let's talk about your project

Healthcare institutions, clinical laboratories, diagnostics manufacturers: write to us to explore how Tucuxi could be set up in your context.

Julien Massari, founder and President LinkedIn profile

Plug'n'Dose SASU · RCS Nanterre 987 993 201 · Courbevoie

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