Globalization enables medical device manufacturers purchasing raw materials and components from China for a high cost-performance. However, it also increases the complexity of the inspection. As an independent and third-party inspection partner, CROXXMORE Medical Device Consulting (CMDC) can conduct a variety of inspections to ensure the compliance and quality of your merchandise.
Pre-Production Inspections
CMDC will inspect raw materials and components before production begins. After product samples are provided, we will verify that the factory has ordered the correct materials, components, and accessories. We will also randomly select and inspect a sample of partially produced products for potential defects, then report our findings to you. If necessary, we can provide the factory with the technical advice necessary to improve product quality and to minimize the chance of defects during production.
During Production Inspections
During Production Inspections are ideal for shipments of substantial quantities; product lines with continuous production; strict requirements for on-time shipments; and as a follow-up if poor results were found during Pre-Production Inspection. Normally, During Production Inspections are carried out when 10-15% of the merchandise is completed. CMDC will inspect the production batch and examine products in the line for possible defects.
At this point we will identify deviations, if any, and offer advice on corrective measures that will ensure uniformity of product and quality. We will also re-check any defects discovered during Pre-Production Inspection and confirm that they have been rectified.
Final Random Inspections
Final Random Inspections can begin only after production has been completed and all merchandise is ready and packed for shipment. Through a statistical method set by industry standards, we will sample products to verify product safety, quantity, workmanship, function, color, size, packing, and more. This ensures that your product is consistent and compliant with all country, industry, or otherwise-specified requirements and that no critical, major or minor defects appear.
