WELCOME TO : Croxxmore Medical Device Consulting

CROXXMORE Medical Device Consulting (CMDC) is your reliable partner in China healthcare market providing sourcing for innovative medical components, devices, instrument and manufacturing solutions. We can help you with sourcing of medical devices for healthcare providers and distributors, a tailored package according to your existing standards and detailed product specifications. We provide supplier auditing for quality manufacturing conforming to ISO13485, ISO9000, CE, FDA compliance with regulatory and environmental regulations. CMDC Sourcing and Manufacturing Service: • Study your products in detail • Review product specifications and determine the number of each item to be sourced • Contact potential suppliers of such products • Write a report summarizing each supplier¡¯s capabilities and ability to make the required products • Discuss the report with the client and answer follow-up questions • Conduct on-site visits the best suppliers to examine QMS systems, etc. • Escort client executives to visit the best suppliers • Negotiate with the suppliers on the client¡¯s behalf as needed • Conclude a sourcing agreement • Monitor sourcing processes post sourcing agreement to make sure products are made correctly and meet the client¡¯s expectations Dual Sourcing & Secondary suppliers De-risking your current supply chain or managing peaks in supply and demand we can be your secondary source for key product lines. We only work with fully accredited suppliers accredited to ISO9000, ISO13485, CE or FDA Quality manufacturing standards. Contract packaging & Bar Coding Our packaging technology includes printing & packaging uniformity, structural packaging, testing and GS1 bar coding for traceability and stock control. Logistics & Supply Chain We integrate into your existing supply chain with CIF or FOB freight services complying with international trade terms. A global solution in the sourcing of medical devices helping you manage your supply chain and sourcing requirements.

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.