In a time when literature reviews have become a critical component of the regulatory process from pre-market approval through post-market surveillance, it is especially important to establish a rigorous and systematic approach for evidence collection and continuous literature surveillance.

DistillerSR, in partnership with Citeline, surveyed global professionals in the medical device and in-vitro diagnostics industry to understand organizational preparedness and management maturity towards literature review practices.

Read the report to gain valuable insights into the importance of investing in new technology and automation to streamline evidence management practices.