Freyr Solutions

8 ভিতরে - অনুবাদ করা

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-

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মন্তব্য করুন

শেয়ার করুন

8 ভিতরে - অনুবাদ করা

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

https://www.ukrpservices.com/

UK Responsible Person Services for Medical Device Manufacturers

Freyr provides UK Responsible Person (UKRP) services to foreign medical device manufacturers for product registration and market entry in the UK.

লাইক

মন্তব্য করুন

শেয়ার করুন

আরো পোস্ট লোড

তথ্য

2 পোস্ট
https://www.freyrsolutions.com/medical-devices
পুরুষ
বাস করছে United States

সম্পর্কিত

Groundbreaking medical innovations are poised to save lives globally, but they are ensnared in the complex web of Regulatory intricacies. Navigating through delayed medical device approvals, compliance challenges, and the constant evolution of requirements can deflate the momentum of your revolutionary device, leaving it stranded on the shores of potential.

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8 ভিতরে - অনুবাদ করা

8 ভিতরে - অনুবাদ করা

UK Responsible Person Services for Medical Device Manufacturers

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