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Medical device manufacturers must comply with record keeping and quality control processes mandated by the Food and Drug Administration (FDA). To comply with these regulations, medical device manufacturers must establish and maintain procedures to ensure that mixups, damage, deterioration, contamination or other adverse effects to products do not occur during handling. The regulations go on to ensure that obsolete, rejected or deteriorated products are not distributed and that items adhere to proper stock rotation. Kardex Remstar automated storage and retrieval systems support the processes demanded by leading medical device manufacturers – from receiving to quality control to manufacturing to distribution and shipping.
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