ipp Dr. Klügl

ipp Dr. Volker Klügl supports medical technology start-ups and innovators in bringing their products to market efficiently and safely. As experienced experts for regulatory requirements (MDR, ISO 13485), we accompany you from the idea to market maturity - with a clear strategy, lean technical documentation and agile processes. So that you can concentrate on innovation.

• Comprehensive regulatory advice.
• Impressive technical documentation.
• Agile project management.
• Process optimization for start-ups and SMEs.
• Easy13485 - the intelligent QMS solution.
• Customized consulting for success

• Regulatory consulting for medical devices (MDR, ISO 13485, QM systems)
• Creation of compliant technical documentation for approval procedures
• Development and implementation of lean, scalable processes for start-ups and SMEs
• Agile project management for product development and approval
• Quality management with the "Easy 13485" QMS solution to ensure ISO 13485 compliance
• Strategic support for clinical evaluations and post-market surveillance processes
• Optimization of audit and certification processes for an efficient market launch