#medicaldevicerrgulatory

Ensuring compliance with UK and EU regulations is a critical part of entering the medical device market. For non-UK manufacturers, navigating these regulations alone can prove challenging and time-consuming. This is where appointing a UK Responsible Person (UKRP) or EU Authorised Representative (EUAR) becomes essential. These roles act as your gateway for regulatory adherence, facilitating smoother market entry and reducing compliance risks.

For more details please visit- https://www.sushvin.com/why-your-business-needs-a-uk-responsible-person-for-medical-device-compliance.html