Real-world evidence (RWE) is becoming increasingly important in the context of health technology assessment (HTA), which is the process of evaluating the clinical and economic impact of healthcare interventions. HTA is used to inform decisions about which treatments, technologies, and interventions should be funded and made available to patients.
RWE can play an important role in HTA by providing additional data on the safety, effectiveness, and cost-effectiveness of healthcare interventions, beyond what is typically available from clinical trials. RWE can be generated from a variety of sources, including electronic health records, administrative claims data, patient registries, and other real-world data sources.
RWE can be used to supplement or replace data from clinical trials, particularly in situations where the clinical trial data is limited or may not fully reflect real-world conditions. For example, RWE can provide information on how interventions work in different patient populations, including those with comorbidities or other conditions that may not have been included in clinical trials.
In addition, RWE can provide valuable information on the long-term effectiveness and safety of interventions, as well as their impact on patient quality of life and other patient-centered outcomes. This information can be particularly important in assessing the value of interventions over the long term and in different patient populations.
Overall, RWE can play an important role in improving the quality and accuracy of HTA, by providing additional data and insights that can help to inform decisions about which healthcare interventions should be funded and made available to patients.
Share this story...
Real World Evidence (RWE) – TMF Reference Model versus the Real-World Study Document Index (RWS-DI)
RWE 101 - TMF Reference Model versus the Real-World Study Document Index (RWS-DI) The Real World Study-Document Index (RWS-DI) is a framework developed by a working group of RWE [...]
Real World Evidence (RWE) 101 – ISF vs TMF
RWE 101 - ISF vs TMF Investigator Site File (ISF) and Trial (Study) Master File (TMF) are key elements in managing clinical and observational studies. They are distinct but [...]
Real World Evidence (RWE) 101 – Study Conduct
RWE 101 - Study Conduct Once the study has been set up, the study conduct phase begins. This phase includes several key activities that ensure the smooth running of [...]
Real World Evidence (RWE) 101 – Monitoring
RWE 101 - Monitoring Monitoring requirements for Real-World Evidence (RWE) studies may differ from those of traditional randomized controlled trials due to the nature of data collection and the [...]
Real World Evidence (RWE) 101 – eConsent
RWE 101 - eConsent Electronic consent or eConsent refers to the process of using electronic systems and processes to convey information related to the study and to obtain and [...]
Real World Evidence (RWE) 101 – Consent to Participate in Research vs Consent to Access and Process Sensitive Healthcare Data (GDPR)
RWE 101 - Consent to Participate in Research vs Consent to Access and Process Sensitive Healthcare Data (GDPR) Consent to participate in research and consent to access and process [...]







