The challenges faced by the medical device industry today have never been greater. Long product life cycles and spiraling manufacturing costs have stifled product innovation and increased financial pressures on medical device manufacturers. At the same time, changing medical needs and regulations across diverse geographies require global solutions to keep pace with rapidly evolving markets.
Infotech provides end-to-end engineering solutions for medical device manufacturers, supporting key product modalities such as patient monitoring systems, diagnostic imaging, therapeutic equipment and in vitro diagnostic equipment. Our innovation-driven design methodologies and process frameworks are carefully designed to improve product innovation, contain costs and reduce time to market.
In addition, our product development processes are in line with ISO 13485: 2003, ISO 14971:2007, ISO 9001:2008, and ISO 27001:2005 requirements ensuring a high level of product reliability and intellectual property security. Equally important is our understanding of different regulatory compliance and homologation requirements, which helps our customers to penetrate emerging markets, address local regulatory requirements and respond quickly to new growth opportunities.
With Infotech as their engineering partner, medical device manufacturers gain experienced and mature product engineering solutions, engineering talent with deep domain knowledge and the proven expertise required to support their ongoing business success in today's competitive marketplace.