Release every IV bag withthe proof.
Molecule, dose and solvent, in 68 seconds.
No laboratory needed, already in more than 60 hospital pharmacies.
Our solution
Two spectra, one verdict. Identity and dose, verified together.
Molecule, concentration and solvent checked on the finished product in under 70 seconds. No dedicated laboratory, no spectroscopy expertise, right in your production unit.
The QCRx® in 3 points
What it changes, in practice.
A 3-in-1 checkMolecule, concentration and solvent verified on the finished product, with every analysis.Understand the QCRx® →
An objective final barrierA measurement on the finished IV bag, free from fatigue or attention bias, at the pace of your releases.See the final barrier →
Built into your workflowResults sent to your prescribing software, automatic archiving, ready for the BPP 2023 batch record.See the workflow →
How it works
A sample goes in, a verdict comes out. No laboratory, within your validation workflow.
- 01Sampling1 mL drawn in the isolator at the end of the preparation.
- 02InjectionThe sample is injected into the QCRx®. The clock starts.
- 03Dual analysisUV spectrum, then Raman spectrum, compared with the molecule's reference.
- 04Verdict in 64 sCompliant or non-compliant, archived and sent to your software.
Control reportExample · chemotherapy bag
Compliant- Preparation
- 5-Fluorouracil 2,400 mg · NaCl 0.9% · 250 mL
- Molecule
- 5-Fluorouracil identified
- Concentration
- 9.5 mg/mL confirmedtarget 9.6 mg/mL · deviation −1.0%
- Solvent
- NaCl 0.9% confirmed
64 s of analysisSent to the prescribing softwareArchived
Why check the finished product
Visual double-checking does not see everything. Analysis measures what the IV bag actually contains.
A dose, molecule or solvent error is invisible to the eye. Only a measurement on the finished IV bag can truly verify it before administration.
Understand the challenges →- 3 out of 7dose errors went unnoticed by visual double-checking in a simulation run at Geneva University Hospitals.
- 40 %of the preparations in this study deviated by more than 5% from the target dose, with or without double-checking.
- 64 sfor a compliant or non-compliant verdict on the finished IV bag, without slowing down releases.
The reference release testing for hospital pharmacies.
1 M+checks per year
60+hospital pharmacies equipped
500+trained users
15 yearsof expertise
They trust us
“Since we started using QCRx®, we release every preparation or batch checked by the system with confidence.”
Dr. Padoin, pharmacist, Martinique University Hospital
See all testimonials →
Support
A partner, not just a supplier. Installation, maintenance, hotline and training: everything is covered.
On-site interventionInstallationOur team installs, configures and qualifies your QCRx® on site, before the first check.
MaintenancePreventive and corrective: we step in before problems arise, and quickly when they do.
HotlineResponsive technical support from Monday to Friday. A question, an incident: we answer.
Training80 h of continuously updated training, with an e-learning platform available 24/7.
Brest University Hospital renews its trust in the QCRx®: a lasting success story
A user of our solution for more than 10 years, Brest University Hospital is investing in a new QCRx®.
Analytical control is not just for dose banding
Dose banding or pure compounding: why analytical control is essential in both cases.
At EAHP 2026 in Barcelona!
The QCRx® was at the largest European hospital pharmacy event, stand no. 102.