Benefits at a Glance
- Part Traceability
- Transaction Accountability
- Pick Accuracy Up To 99.9%
Solutions from Alternative Handling Technologies
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.