Medical Device Fluid Dispensing Systems
The SmartDispenser® Reduces Complexity of Equipment Validation
Enterprise-Wide Fluid Dispensing Standardization – Medical products must meet regulatory requirements of the U.S. Food and Drug Administration (FDA), European Union Medical Devices Directive and other governing agencies worldwide for quality and product consistency. All materials and manufacturing procedures for pharmaceutical, medical device and diagnostics equipment must be documented for complete traceability and process validation. In addition, there are required audit trails, closed-loop corrective action plans and automated data capture related to product issues and defects.
Therefore, the challenge for medical device manufacturers is to find ways to increase efficiency in their processes in order to remain competitive while staying compliant with the various regulatory bodies governing world markets.
