
About
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.

