Tag: FDA drug listing services

XPRO America – US FDA Drug Establishment Registration (21 CFR Part 207)

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The US FDA Drug Establishment Registration is a mandatory requirement under 21 CFR Part 207 for all facilities engaged in the manufacturing, repacking, relabeling, or distribution of human and veterinary…

XPRO America – FDA Annual & Ongoing Compliance Services for Drug Firms

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For companies manufacturing, repacking, relabeling, or distributing human and veterinary drugs, annual and ongoing compliance with the U.S. Food and Drug Administration (FDA) is a mandatory responsibility. Non-compliance can lead…