CE Marking

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Finesse Medical can assist you in CE marking your medical devices. We can generate or assist in compiling the required documentation for CE marking including:

• Clinical expert reports.
• Product and process risk analysis .
• Sterilisation Validation documentation.
• Shelf life studies.
• Biocompatibility testing.
• Vendor Auditing.
• Compliance with essential requirements.
• Notified body submission.