MARACA International has announced it will be presenting its services at the MedTech Summit Meeting, Brussels.

Taking place from 11 June to 15 June in at the Hotel NH Brussels Bloom, the MedTech Summit Meeting is a medical device and in-vitro diagnostic devices (IVD) conference providing medical device manufacturers with networking opportunities.

If you have questions about the new Medical Device Regulation (MDR) or In Vitro Diagnostic Devices Regulation (IVDR) and their impact on your company, make an enquiry using the form on this page and MARACA will get you on the right track.

MARACA International is a Belgian consulting company providing service excellence for regulatory, quality, clinical and medical affairs assignments for medical device, IVD and pharmaceutical companies, as well as clinical laboratories, notified bodies and governmental agencies.

These services support your product registrations in Europe under the MDD, IVDD, MDR and IVDR regulations. In the US, MARACA’s services support your submissions to the US Food and Drug Administration (FDA). The company’s services include training, quality system management, risk management, development of design dossiers and technical files, registration of devices, clinical evaluation reports, scientific validity reports and post-market follow-up plans and reports.