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Global Unique Device Identification Database (GUDID) for the Healthcare Industry
Is the GUDID Deadline Approaching for Your Class?
Like most industries, Healthcare is changing rapidly! For example, Healthcare has the added accountability to government agencies, associations, and patient advocates who are spearheading and mandating change under the guides of “Improved Patient Safety”.
The US Food & Drug Administration (FDA) will ultimately require Medical Devices manufacturers of all Classes under UDI Rule: 78 FR 58785 to comply with the implementation of the GUDID.
Haskins Advisory Group can get you there… whether you’re a GDSN customer or need to go direct via the FDA’s web interface or HL7/SPL. We have expertise in these areas, having helped other labelers; we can help you meet compliance for your medical devices!
Need Help With Your Healthcare GUDID Project?