Real-world data (RWD) and real-worldevidence (RWE) played an increasing role inhealthcare decisions. The 21st Century Cures Act, passed in 2016, placed additional focus on the use of these types of data to support regulatory decision making. Here’s why RWE is becoming a game-changer: 1. Real Insights from Real Patients: Unlike traditional randomized controlled trials (RCTs), RWE studies involve real patients in real-world settings. This provides a more comprehensive view of health outcomes and patient experiences. Both RWD and RWE are essential concepts in the pharmaceutical industry, but they have distinct meanings. RWD is the data gathered from real-life healthcare interactions and comes from outside clinical settings. In this video David Thompson, Syneos Health, provides his thoughts on the role of real-worldevidence (RWE) inhealthcare decision making. Real-worldevidence (RWE) refers to data collected from sources other than traditional randomized clinical trials (RCTs), such as observational studies, electronic health records, and patient registries. Real-worldevidence (RWE) is increasingly being used to improve access to healthcare in remote areas. In India, RWE has been used to evaluate the impact of the National Health Insurance Scheme on healthcare utilization and financial protection. Real-WorldEvidence (RWE) is based on the analysis of real-world data (RWD), such as electronic health records (EHR), medical claims, and wearable-generated data, to generate clinical evidence.

You may also like