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United Kingdom Responsible Person MHRA Requirement

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1 year 4 months ago #355 by James Cox
United Kingdom Responsible Person MHRA Requirement was created by James Cox
Did you know that even seemingly simple products like spectacle frames and dry eye glasses are classified as medical devices? Under the MDD and MDR, all ophthalmic products require registration with the MHRA, including those imported from the EU or elsewhere.

Avoid costly delays and penalties by ensuring your products are compliant. IgniteQA, your trusted ophthalmic quality and regulatory consultancy, can help.

Here's how we support you:

Act as your UK Responsible Person: We'll be your liaison with the MHRA, streamlining the registration process.
Register individual practices as importers: We take care of the paperwork so you can focus on your business.
Verify manufacturer or distributor compliance: Use our expertise to check the MHRA Public Database and avoid any issues.
Don't risk penalties or product recalls! Contact IgniteQA today at jim@igniteqa.com to discuss your specific needs and ensure smooth sailing for your ophthalmic products.

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