Tag: RWE

Data Sources: EMR/EHR, Claims, PROs: Best Practices for High-Validity Real-World Evidence

November 23, 2025November 18, 2025 digi

Data Sources: EMR/EHR, Claims, PROs: Best Practices for High-Validity Real-World Evidence Data Sources: EMR/EHR, Claims, PROs: Best Practices for High-Validity Real-World Evidence The emergence of Real-World Evidence (RWE) is reshaping the landscape of clinical trials and observational studies. Regulators like the FDA and EMA emphasize the importance of RWE in corroborating clinical outcomes and therapeutic…

Data Sources: EMR/EHR, Claims, PROs

How to Design Data Sources: EMR/EHR, Claims, PROs for FDA, EMA and HTA Acceptance

November 23, 2025November 18, 2025 digi

How to Design Data Sources: EMR/EHR, Claims, PROs for FDA, EMA and HTA Acceptance The advent of real-world evidence (RWE) has significantly changed the landscape of clinical research, especially in the context of how data sources such as Electronic Medical Records (EMR), Electronic Health Records (EHR), claims data, and patient-reported outcomes (PROs) are utilized. This…

Data Sources: EMR/EHR, Claims, PROs

Data Sources: EMR/EHR, Claims, PROs in Practice: Step-by-Step Guide for Real-World Researchers

November 23, 2025November 18, 2025 digi

Data Sources: EMR/EHR, Claims, PROs in Practice: Step-by-Step Guide for Real-World Researchers Data Sources: EMR/EHR, Claims, PROs in Practice: Step-by-Step Guide for Real-World Researchers Introduction to Real-World Evidence in Clinical Research Real-World Evidence (RWE) is increasingly recognized as a vital component in the development and regulatory evaluation of treatments. This guide is designed for clinical…

Data Sources: EMR/EHR, Claims, PROs

Common Biases in Data Sources: EMR/EHR, Claims, PROs—and How to Correct Them

November 23, 2025November 18, 2025 digi

Common Biases in Data Sources: EMR/EHR, Claims, PROs—and How to Correct Them Common Biases in Data Sources: EMR/EHR, Claims, PROs—and How to Correct Them In the burgeoning field of clinical research, the utilization of real-world data (RWD) has significantly transformed our understanding of medical practices. However, biases in data sources such as electronic medical records…

Data Sources: EMR/EHR, Claims, PROs

Aligning Data Sources: EMR/EHR, Claims, PROs With Regulatory and HTA Expectations

November 23, 2025November 18, 2025 digi

Aligning Data Sources: EMR/EHR, Claims, PROs With Regulatory and HTA Expectations In the context of contemporary clinical research, the integration of various data sources—such as Electronic Medical Records (EMR), Electronic Health Records (EHR), claims data, and Patient-Reported Outcomes (PROs)—has emerged as a focal point of interest among clinical and regulatory professionals. Effective alignment of these…

Data Sources: EMR/EHR, Claims, PROs

Governance, Ethics and Compliance Considerations for Study Designs: Cohort, Case-Control, Registry

November 23, 2025November 18, 2025 digi

Governance, Ethics and Compliance Considerations for Study Designs: Cohort, Case-Control, Registry Governance, Ethics and Compliance Considerations for Study Designs: Cohort, Case-Control, Registry In the realm of clinical research, particularly when dealing with observational studies, decisions surrounding study design are paramount. Understanding the ethical implications and structured governance is crucial, especially in the context of cohort,…

Study Designs: Cohort, Case-Control, Registry

Statistical Approaches to Strengthen Study Designs: Cohort, Case-Control, Registry

November 23, 2025November 18, 2025 digi

Statistical Approaches to Strengthen Study Designs: Cohort, Case-Control, Registry In the constantly evolving field of clinical research, the integrity and reliability of study designs are paramount. As clinical operations, regulatory affairs, and medical affairs professionals, understanding the statistical approaches inherent in various study designs such as cohort, case-control, and registry studies is essential. This tutorial…

Study Designs: Cohort, Case-Control, Registry

Operationalizing Study Designs: Cohort, Case-Control, Registry Across Global Programs

November 23, 2025November 18, 2025 digi

Operationalizing Study Designs: Cohort, Case-Control, Registry Across Global Programs Operationalizing Study Designs: Cohort, Case-Control, Registry Across Global Programs In today’s rapidly evolving clinical research landscape, understanding the operational nuances of various study designs is crucial for optimizing real-world evidence (RWE) initiatives. This guide aims to meticulously delineate the processes required for implementing cohort, case-control, and…

Study Designs: Cohort, Case-Control, Registry

How AI and Automation Are Transforming Study Designs: Cohort, Case-Control, Registry

November 23, 2025November 18, 2025 digi

How AI and Automation Are Transforming Study Designs: Cohort, Case-Control, Registry How AI and Automation Are Transforming Study Designs: Cohort, Case-Control, Registry The landscape of clinical trials has been undergoing a revolution fueled by advancements in artificial intelligence (AI) and automation. This transformation is particularly evident in study designs employed in real-world evidence (RWE) and…

Study Designs: Cohort, Case-Control, Registry

Future Trends: Real-World, Digital and Hybrid Evidence in Study Designs: Cohort, Case-Control, Registry

November 23, 2025November 18, 2025 digi

Future Trends: Real-World, Digital and Hybrid Evidence in Study Designs: Cohort, Case-Control, Registry Future Trends: Real-World, Digital and Hybrid Evidence in Study Designs: Cohort, Case-Control, Registry In the landscape of clinical research, understanding and harnessing real-world evidence (RWE) has become increasingly paramount. With the ever-evolving methodologies and regulatory frameworks, professionals in clinical operations, regulatory affairs,…

Study Designs: Cohort, Case-Control, Registry