Diversity in the context of real-world research refers to the inclusion of individuals from different backgrounds, including but not limited to race, ethnicity, gender, age, sexual orientation, socioeconomic status, and geographic location. It is important to ensure diversity in research because it can provide a more comprehensive understanding of health and healthcare outcomes, as well as enable the development of interventions that are effective for all populations.
In the past, research has often focused on populations that are easier to access, which has led to underrepresentation of certain groups in research studies. This lack of diversity can result in biased and incomplete research findings that do not accurately reflect the experiences and health outcomes of all populations.
Therefore, it is crucial for real-world research to include diverse populations to ensure that research findings can be generalized to all groups. This can help to identify health disparities, understand the root causes of these disparities, and develop interventions that are effective for all populations.
In summary, diversity in real-world research means including individuals from diverse backgrounds to ensure that research findings are inclusive, representative, and generalizable to all populations. By doing so, research can more effectively identify and address health disparities and improve health outcomes for all individuals.
Share this story...
Real World Evidence (RWE) 101 – ICH GCP (R3) – Real World Evidence Context
RWE 101 - ICH GCP (R3) - Real World Evidence Context Revision 2 of ICH GCP caused confusion to those of us who work with non-interventional studies. The glossary [...]
Real World Evidence (RWE) 101 – Non-Interventional Studies vs Market Health Research
RWE 101 - Non-Interventional Studies vs Market Health Research Key differences between a non-interventional study (NIS) and market health research include:1. Research Objective: NIS are conducted to examine real-world [...]
Real World Evidence (RWE) 101 – Real World Evidence (RWE) 101 – Audits vs Inspections
RWE 101 - Real World Evidence (RWE) 101 - Audits vs Inspections In the context of regulatory compliance for Real-World Evidence (RWE), both audits and inspections play crucial roles, [...]
Real World Evidence (RWE) 101 – A Career of Many Pathways
RWE 101 - A Career of Many Pathways Real-world evidence (RWE) refers to the information on health care that is derived from analysis of real-world data (RWD). RWE [...]
Real World Evidence (RWE) 101 – Evolution of Regulatory Affairs
RWE 101 - Evolution of Regulatory Affairs Real-world evidence (RWE) and real-world data (RWD) are increasingly influencing regulatory affairs in the biopharmaceutical and healthcare industry. This change has been [...]
Real World Evidence (RWE) 101 – Project Managers
RWE 101 - Project Managers Real-World Evidence (RWE) observational studies and clinical trials are both key elements of medical research, but they involve very different methodologies, aims, and requirements. [...]