MHRA UK Responsible Person Registration Overview

UK MHRA mandates Medical Device manufacturers located outside the United Kingdom (UK) and without any local business offices for MHRA UK Responsible Person registration. Manufactureres need to appoint a United Kingdom Responsible Person (UKRP) or UK Representative on their behalf, as a pre-requisite for device registration and launch of the device in the United Kingdom.

https://www.ukrpservices.com/a....-step-by-step-guide-

UK Responsible Person Toolkit
Avail a complete set of guidance documents, templates and exhaustive checklists to ensure successful device registration

https://www.ukrpservices.com/

Software as Medical Device (SaMD), also called Medical Device Software (MDSW) is the latest booming topic in the healthcare segment. The global SaMD market is estimated to be valued at US $86.5 billion by 2027, at a CAGR of 21.9% from 2020 to 2027. This growth is triggered by various factors of SaMD compliance such as, adoption of Internet of Things (IoT), digital healthcare platforms and adoption of software for continuous monitoring of physiological parameters by healthcare providers for remote assistance.

https://www.freyrsolutions.com..../medical-devices/sof

https://www.freyrsolutions.com/medical-devices

Freyr, as a proven Regulatory partner, provides end-to-end Medical Device Regulatory services that span across decoding Medical Device classification, compiling Device documentation, Medical Writing, Device Registration and acting as an in-country representative.