Amelia Winslete

3 jr - Vertalen

Medical Device Regulatory Consultant

Medical Device Regulatory Consultants - I3CGlobal (UK)

www.i3cglobal.uk

Medical Device Regulatory Consultants - I3CGlobal (UK)

To be an independent, credible, and professional medical device regulatory consultant who treats all our customers fairly in our dealings with us.

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Delen

3 jr - Vertalen

EU Authorised Representative
#eurepresentative #euauthorisedrepresentative #medicaldevices

EU Representative: Best EU Authorised Representative for medical devices

www.i3cglobal.uk

EU Representative: Best EU Authorised Representative for medical devices

Medical Device Manufacturers that don’t have a physical location in Europe must appoint a eu authorised representative who is located within Europe. EU Representative is mandatory for EU MDR & IVDR Medical Device CE Marking.

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Delen

3 jr - Vertalen

UKCA Mark Certification for Medical Devices
#medicaldevices #ukca #ukcamark #ukcacertificate

UKCA Mark Certification - Medical Device Regulation in the UK

www.i3cglobal.uk

UKCA Mark Certification - Medical Device Regulation in the UK

UKCA mark certification is known as UK product marking that will be needed for products placed on the Great Britain market. Contact us for UKCA certification technical support service for medical and IVD devices.

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Delen

3 jr - Vertalen

CE Mark for medical devices
#medicaldevices #cemark

CE Mark for Medical Devices - Excellent Service Provider

www.i3cglobal.uk

CE Mark for Medical Devices - Excellent Service Provider

CE mark for medical devices stands for Conformité Européenne and this is a legal requirement to place the medical device on the market in Europe.

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3 jr - Vertalen

FDA 510(k) Submission & approval & documentation services
#fda #510k #fda510k #medicaldevices

FDA 510k Consultant for Documentation, Submission & Approval

www.i3cglobal.uk

FDA 510k Consultant for Documentation, Submission & Approval

To ensure a successful 510(k) submission and clearance, the role of 510k consultant is very much vital. The services that we provide customers to reduce the cost, duration, and failures in 510k submission.

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