Verify UKRP Status - I3CGLOBAL (UK)

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I3CGLOBAL (UK)

Medical Device Consultants in UK

+44 75 8147 1399
enquiry@i3cglobal.uk

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OUR TEAM
UKCA MARK
EU CE MARK
US FDA
- FDA 510(k)
  - STERILIZATION PROCESS
  - SOFTWARE DEVICE 510K PROCESS
- FDA REGISTRATION
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CONTACT US

HOME
OUR TEAM
UKCA MARK
EU CE MARK
US FDA
- FDA 510(k)
  - STERILIZATION PROCESS
  - SOFTWARE DEVICE 510K PROCESS
- FDA REGISTRATION
BLOG
CONTACT US

VERIFY UKRP AGREEMENT STATUS

Organisation First Name:

Our Company

I3CGlobal (UK) helps organizations to overcome regulatory hurdles by sharing, guiding, training and developing documents that of high quality, economically viable and assurance of clearance .

As knowledge driven team that aims to be strategic outsourced partners to customers, we strive to build an good long lasting tie up with every customers who provide business to us. Continue to be curious and constantly educate our self in new ways of solving new regulatory requirements .

One step ahead. All the time.