ServiceUpdated on 21 April 2026
Software development in line with regulatory frameworks
Business Development at VIALUTIONS consult GmbH
Berlin, Germany
About
We support MedTech and HealthTech companies, as well as organizations operating in regulated Pharma and laboratory environments (GLP) across the DACH region with software development, modernization, and maintenance.
We work in line with regulatory frameworks such as MDR, ISO 13485, and IEC 62304, with a strong focus on data integrity, auditability, and traceable processes.
We work within existing QMS frameworks – not alongside them.
Organisation
Similar opportunities
Partnership
Join the TraceX Founding Partner Program
- Others
Charles Rollet
CEO and Cofounder at TraceX
CLICHY, France
Expertise
Regulatory Affairs Specialist (MDR, ISO 13485)
- Quality and knowledge management
Lesley Plön
Consultant Regulatory Affairs at Johner Institut GmbH
Konstanz, Germany
Product
- Software
- Distribution Partner
- IT for medical technologies
- Quality and knowledge management
Antonina Burlachenko
Head of Regulatory Consulting at Star
Wroclaw, Poland