Good Distribution Practice (GDP) isn't exclusive to pharmaceuticals; medical devices and supplies need similar controls during storage and transport to preserve their safety and effectiveness until they reach the end user in the same condition they left the factory.
A properly registered device can still lose its actual conformity if exposed to improper storage or transport conditions — and the authority may treat this as a violation entirely independent of the product's registration status.
Documenting GDP procedures as a written internal policy — rather than an unwritten practice passed between staff — makes any inspection or unannounced review from the authority far easier to handle.
Investing in disciplined storage and distribution practice protects a larger investment: the product's registration itself, and the establishment's standing with the regulator.
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