In the face of increased quality issues and the high costs of maintaining compliance, Medical Devices organisations face significant challenges in advancing product quality and still meeting the demands of growing the bottom line and overall business profitability. These challenges are present across various phases of the product development life-cycle including planning, design, supply, manufacturing, and customer support. Most often resolution of the issues presenting are approached in technology silos resulting in islands of automation and disjoint information systems, which are neither optimised for the users nor provide optimum functionality for the business process.
CXV Global is an ideal partner to help Medical Device manufacturers design and develop products that meet industry connectivity and interoperability requirements and standards. Our solutions comprise of design, hardware, software, support and training services and provide compliance with industry regulations including FDA CFR 21 Part 11 and GAMP standards. Our solutions and services are geared towards reducing development costs, improving time to market, and reducing the barriers to market entry.
The production and distribution of medical devices is highly regulated. Driven by patient safety, vision inspection is employed widely throughout the manufacturing to guarantee product quality, reduce recalls and comply with regulations around traceability, namely the Unique Device Identification (UDI).
We’ve been leading the way in the solutions we bring to customer problems and in the deployment of leading edge technologies for over 30 years.