As clinical trials become more global and patient-centered, capturing patient experiences accurately across diverse populations is crucial. Electronic Patient-Reported Outcomes (ePRO) offer significant advantages over
???? What is Real-World Data? Real-world data (RWD) refers to health information gathered outside the controlled settings of clinical trials, such as from electronic health
Reducing Respondent Burden in Patient-Reported Outcome (PRO) Data Collection ???? In this whitepaper, you’ll find: Strategies for minimizing respondent burden during PRO data collection Methods
How Psychometrics Influence PRO Selection for Clinical Trials ???? In this whitepaper, you’ll find detailed insights on: The importance of psychometrics in selecting Patient-Reported Outcomes
Key Components of a Clinical Evaluation Report: Essential Sections and Their Content ???? In this whitepaper, you’ll find detailed insights on: The expected structure of
Reforming Clinical Evaluation of Medical Devices in Europe In this whitepaper, you’ll find detailed insights on: The clinical evaluation process for medical devices, including pre-
A Comprehensive Guide to Clinical Investigations with Medical Devices in Europe: Pre- and Post-Market Requirements ???? In this whitepaper, you’ll find detailed insights on: The
SAE Reporting in Germany: A Guide for Clinical Investigations under MDR 2017/745 ???? In this whitepaper, you’ll find detailed insights on: The requirements for reporting
Mastering Vigilance Reporting Requirements in Germany: A Guide for MedTech Professionals ???? In this whitepaper, you’ll find detailed insights on: Vigilance reporting obligations under MDR
