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REGUFLOW

ReguFlow

Digital support in medical device manufacturing regulation -  the development of ReguFlow has begun

Goroid Ltd. is implementing a new project "ReguFlow - Effective cloud-based, MDR-compatible support for the regulatory and manufacturing challenges of medical device manufacturers" with the help of a non-refundable grant within the framework of the Széchenyi Plan Plusz program.
 

The project aims to develop the ReguFlow software platform, which provides comprehensive support to small and medium-sized enterprises (SMEs) manufacturing custom-made medical devices, ensuring compliance with the EU Medical Device Regulation (MDR) 2017/745. Effectively supporting the areas of technical documentation, quality management systems and post-conformity verification, etc. Building on the company's previous digital development activities, ReguFlow contributes to the digital convergence of SMEs in the domestic and European healthcare industry.
 

The project is implemented within the framework of DIMOP Plusz-1.1.2/A-24 the Dedicated R&D&I and market entry support program for digital economy players - Digital product innovation developments call, with the support of the European Union and co-financing from the Hungarian state.

FUND DETAILS

EU FUND

details

Beneficiary:   Goroid Ltd.
 

Project ID number:   DIMOP_PLUSZ-1.1.2/A-24-2025-00274
 

The subject of development:   ReguFlow - Effectively supporting the regulatory and manufacturing challenges of medical device manufacturers
 

Amount of contracted support:    34.780.000 HUF
 

Planned completion date:    July 2026 

The project is implemented with the support of the European Union and co-financed by the Hungarian state.

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