August 13, 2013

Best Practices for Managing Medical Device Development Risk

Community
wp_exposerisk_174x212Identifying, assessing, and tracking safety risk in the product development process is an incredibly time-consuming task that rarely gets the attention it requires. To help medical device development organizations reduce the time spent on risk management, we just released a new white paper entitled “Exposing Risk Throughout Your Product Development Lifecycle.” The free, downloadable white paper offers best practices on using traceability to analyze, identify, and control safety risks throughout the product development lifecycle. Organizations that use traceability-based risk management can reduce the time spent on risk management by focusing on traceability between requirements and corresponding risk controls, according to Seapine’s industry experts. The white paper goes hand-in-hand with the 2013 State of Medical Device Development Survey, sponsored by Seapine Software. Over 300 life sciences professionals have already shared their design, risk, and quality control experiences via the survey, which runs through August 31. To download the white paper, visit www.seapine.com/exposing-product-risk.