Understand
Review goals, processes and data together. Identify the use case with the greatest potential value.
PRODUCT DATA & REGULATORY · SWITZERLAND
Control your product data.
Keep regulation in view.
Aras PLM, regulatory data and product information for companies in Switzerland. From engineering through swissdamed and EUDAMED to ongoing operations.
INTELLIGENT SOLUTIONS. LASTING VALUE.VALNARO AG · SWITZERLAND
ARAS PLMRIM · PIM · DPPENTERPRISE INTEGRATIONSUPPORT & OPERATIONS
01 / SOLUTIONS
From scattered data
to a shared picture.
From development to the product passport, we connect your information, processes and systems.
RIM
Regulatory Information
Structure regulatory information to support approvals and registrations.
Explore solutionPIM
Product Information
Create consistent product information for sales, service and digital channels.
Explore solutionDPP
Digital Product Passport
Connect product, material and supplier data in a traceable information foundation.
Explore solutionCEI
Enterprise Integration
Connect PLM, ERP and other business systems through clearly defined interfaces.
Explore solutionRIM / SWISSDAMED & EUDAMED
One body of data.
Multiple markets.
UDI, product records and approvals belong together. We design RIM data models and workflows with Swiss registration in swissdamed and the requirements of your other markets in mind.
Explore RIM for Switzerland
02 / SERVICES
From the first question
to a solution that lasts.
A good solution fits your processes. We combine business understanding, software and integration with an architecture that can evolve.
Our servicesThree starting points. One connected product process.
01
Aras Innovator
From the first PLM structure to the next upgrade. We work with you to plan Aras processes, integrations and application operations.
Explore the offering02Support & operations
Already running Aras or a RIM, PIM or DPP solution? Start with the current system: application, responsibilities, outstanding issues and the next planned change.
Explore the offering03Medtech & life sciences
From engineering to market registration: product data must be consistent, changes traceable and responsibilities clear.
Explore the offeringOUR APPROACH
Clear in our thinking.
Committed in delivery.
Connect
Design a suitable architecture and test it in a focused pilot. Share what we learn early.
Evolve
Expand the solution step by step. Consider operations, knowledge transfer and new requirements from the start.
03 / VALNARO
Intelligent solutions.
Lasting value.
VALNARO AG is your contact in Baar for product data, Aras PLM and regulatory information processes. Our consulting, implementation and system development services focus on the Swiss market.
VALNARO AG, formerly mediatec.net Switzerland AG, is based in Baar. The name change was published in the Swiss Official Gazette of Commerce on 25 August 2026.
Get to know VALNAROInsights
DPP readiness check
11 / 2026DPP data quality: five checks before publication
A product passport can be technically accessible and still contain incorrect information. For Swiss manufacturers exporting to the EU, a review of its content before publication is a useful step. Five questions connect engineering, purchasing and IT data with a traceable decision: is this information ready to share?
10 / 2026Item numbers, UDI and CHRN: connect the right identifiers
The ERP holds an item number, the package carries a UDI and the actor registration contains a CHRN. Which identifier belongs in which field? For Swiss medtech companies, reliable RIM integration starts with that mapping. Combining different meanings in a single “product ID” field creates avoidable ambiguity between regulatory affairs, production and IT.
10 / 2026The EU DPP Registry: data responsibilities for Swiss exporters
A Swiss manufacturer is preparing product information for the EU market. The team is discussing registration, while material evidence, technical data and service documents remain spread across different systems. Who will keep the product passport reliable over time? Start by assigning clear responsibilities for source data, publication and ongoing operations.
10 / 2026swissdamed: reconcile product changes under control
Initial registration is followed by ongoing data maintenance. For Swiss manufacturers and authorised representatives, an approved product change needs to reach the right register. This workflow helps make the connection between business ownership, RIM and technical interfaces verifiable.
09 / 2026EUDAMED & swissdamed: data readiness
Two registries, shared source data. Start with product records and responsibilities before automating an export.
09 / 2026swissdamed: a guide to preparing your data
A practical checklist for Swiss manufacturers and teams responsible for registration data.
09 / 2026CSV: validation by intended use and risk
Computer system validation starts with the quality-related task a system is intended to perform. This working structure helps you plan with QA.
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