Arianis brings inventory, protocols, production and traceability together in a light, user-friendly interface, built for laboratories and regulated industries: medical devices, in vitro diagnostics, biotechnology, dietary supplements, medical nutrition...
In laboratories and regulated industries, running things on Excel or on ill-suited software is not unusual. Scattered data and manual tracking have a direct impact on quality and compliance.
Arianis doesn't replace your business logic: it gives it structure. Numbering, units, locations, label formats: everything is configured to your rules.
Auto-filled fields, QR/barcode scanning from a smartphone, one-click actions: recurring operations no longer slow your teams down.
A clean interface, contextual navigation, the right information in the right place at the right time. Your teams find what they need without tedious training.
A central dashboard, proactive alerts, exportable data. Key information surfaces on its own, without any digging.
List consumables, reagents, tools and equipment. Track quantities, expiry dates and locations. Get alerts before critical thresholds are reached.
A clear dashboard and notifications to see and follow how quantities change, spot stock below threshold and anticipate expiry dates. Critical equipment and its metrology checks are tracked too.
Rely on protocols to standardize every operation. Record consumption, justify deviations, approve quantities. Export the complete batch release record in one click.
Each production run follows a defined protocol, with the stock and equipment it requires. The system flags deviations, lets you justify them, and generates a complete, exportable summary sheet.
The platform centralizes data, makes records reliable and gives you a clear view to make better decisions, faster.
Instantly find which lots were affected by a deviation, a faulty piece of equipment or a change of supplier. Forward and backward traceability is structured, navigable and exportable.
Each module is designed to work with the others, from raw stock to the shipment of the packaged lot.
Follow the life cycle of your equipment and manage your consumables inventory. Expiry alerts, metrology and a complete consumption history.
Define your manufacturing recipes: consumables, required equipment and the associated quality control levels.
Protocol-guided data entry, deviation justification, pre-labeling, printable sheets and exportable batch records. The lots you produce feed directly into your other production runs.
Make quality control of production runs mandatory, and document conformities and non-conformities. Some protocols can be exempted from approval (R&D, etc.).
Serialize your units, manage multi-level packaging, generate your UDI labels to meet MDR 2017/745 requirements, and release your batches.
Generate your delivery notes and keep full track of where each lot you produce ends up.
Separate production sites or activities, or keep production and R&D apart.
Record your production sheets, approvals and conformity checks. Attach your evidence and supporting documents to the records, then export your data as CSV.
Pre-reserve lot numbers and generate multi-format labels (barcodes, QR codes, etc.) tailored to your business. Serialize your conforming products and generate UDI labels.
Forward and backward navigation across the whole life cycle of a lot, from raw material to end customer.
Every action is recorded with a timestamp and the operator's identity. A complete history you can actually use.
A central view of critical alerts, expiry dates, equipment due for checks and stock trends.
Arianis is not a general-purpose ERP. It is a tool cut out for the constraints of regulated environments, with the usability your shop-floor teams deserve.
Works on a computer, a tablet or a smartphone. Built-in barcode scanning. No hardware setup required.
SSL/TLS-encrypted connections, a dedicated and isolated instance, daily backups, fine-grained permissions per module and per user.
Custom internal numbering, label formats, units of measure, stock locations: everything adapts to your business rules.
Native CSV exports to feed your existing business tools. Production sheets, batch records and delivery notes generated automatically as PDFs, ready to flow through your processes as they are.
Designed for ISO 13485, MDR 2017/745, GxP and 21 CFR Part 11 requirements. Compliance becomes an operational asset, not a burden.
The Cerebellis team takes care of deployment, configuration and onboarding. We are here to support you, and we can design custom modules for your specific needs: Arianis grows with you.
“For a medical device manufacturer like us, Arianis is perfect. It's the inventory / production management software we needed: easy to get started with, and it meets our expectations exactly. Inventory management, quality controls, traceability, deviation / non-conformity management, lot and serial numbers: Arianis helps us at every stage of production and development. It's simple and efficient to use, and I can only recommend it.”
In regulated environments, deploying new software is not something you improvise. We support you at every step of qualification or CSV (Computerized System Validation), so that your go-live is compliant, documented and audited.
We help you structure your qualification approach: validation plan, scope definition, IQ/OQ/PQ test levels according to your regulatory requirements (ISO 13485, GxP, 21 CFR Part 11).
Our teams help write and run the test protocols: use cases, test scenarios, anomaly management and requalification. You save time and gain rigor.
Qualification report, traceability matrices, anomaly summaries: we help you produce the deliverables your auditors expect, ready to slot into your QMS.
Let's build the offer together.
Let's talkStart without any commitment — your pilot at €990 excl. VAT for three months on a real scope, with our support. At the end of the three months, you are free to subscribe or to stop, and your data remains exportable.
Start my pilot10 in-depth guides on the questions that come up in audits, during lot recalls and when choosing a tool.
The eight questions that always come up. The full FAQ covers about twenty.
A 15-minute call is enough to see whether the platform fits your context.