Every day, companies face medical device compliance realities and responsibilities associated with developing, producing, and distributing products that improve quality of life.
To be successful, they continually need to produce innovative products that are clinically and economically relevant while facing strict regulatory requirements, increasing competition and demanding time-to-market and cost pressures. However, many companies operate in silos. Different groups including Regulatory Affairs/Quality Assurance (RA/QA), project and product managers conduct product development and regulatory compliance functions using different information systems and long-established, disjointed manual and paper-based processes.
Download our expert whitepaper Beyond Compliance: Connecting the Dots Between Quality, Engineering and Regulatory to Increase Innovation & Improve Operational Efficiency to learn more.