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I3CGLOBAL (UK)
Medical Device Consultants in UK
+44 75 8147 1399
enquiry@i3cglobal.uk
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ABOUT US
UKCA MARK
UK RESPONSIBLE PERSON (UKRP)
UKCA MARKING
VERIFY UKRP STATUS
EU CE MARK
EU REPRESENTATIVE
MEDICAL DEVICE CE MARKING
TECHNICAL FILE MEDICAL DEVICE
CLINICAL EVALUATION REPORT
PERIODIC SAFETY UPDATE REPORT
IN VITRO DEVICE CE MARKING
IVDR CLASSIFICATION
IVDR TECHNICAL FILE
PERFORMANCE EVALUATION REPORT
ISO 13485 Certification
MEDICAL SOFTWARE CE MARKING
US FDA
FDA 510(k)
STERILIZATION PROCESS
SOFTWARE DEVICE 510K PROCESS
FDA REGISTRATION
BLOG
CONTACT US
HOME
ABOUT US
UKCA MARK
UK RESPONSIBLE PERSON (UKRP)
UKCA MARKING
VERIFY UKRP STATUS
EU CE MARK
EU REPRESENTATIVE
MEDICAL DEVICE CE MARKING
TECHNICAL FILE MEDICAL DEVICE
CLINICAL EVALUATION REPORT
PERIODIC SAFETY UPDATE REPORT
IN VITRO DEVICE CE MARKING
IVDR CLASSIFICATION
IVDR TECHNICAL FILE
PERFORMANCE EVALUATION REPORT
ISO 13485 Certification
MEDICAL SOFTWARE CE MARKING
US FDA
FDA 510(k)
STERILIZATION PROCESS
SOFTWARE DEVICE 510K PROCESS
FDA REGISTRATION
BLOG
CONTACT US
VERIFY UKRP AGREEMENT STATUS
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