The global medical device industries are facing challenges such as time to market, Innovative design with competitive cost and increasing the product development cost.
CADTECH engineering practice helps our partner in developing innovative products through our complete product life cycle capabilities from concept design to manufacturing. We help our partners to meet product cost target, Optimize development cost, solve product sustenance challenges through product engineering and product regulatory compliance support for various geographies.
We adopt stringent process control and conform to regulatory standard to ensure faster time to market. Our mature processes meeting the requirements of ISO 13485:2003, ISO 9001:2008, ISO/IEC 27001 and IP standards.