Considerations for Transitioning from Paper to eSource
Switching from paper to eSource in clinical trials enhances data accuracy, reduces errors, and boosts organization, offering more efficient study management.
Switching from paper to eSource in clinical trials enhances data accuracy, reduces errors, and boosts organization, offering more efficient study management.
A clinical research trial can only be as strong its participant population, but it’s challenging to find eligible patients.
Dawn Wydner, former Food and Drug Administration (FDA) Consumer Safety Officer, LCDR, and current Managing Expert for Advarra’s Quality Center
Phase I oncology trials present distinct ethical challenges, such as participant vulnerability and the risk of therapeutic misconception, requiring careful oversight.
As March 2020 completely disrupted any sense of normalcy, including in the workplace, many were forced to adapt rather quickly.
As a research site starts the adoption and implementation process for a new technology, there are several moving parts. Sites
Since early 2020, clinical research sites – like many industries – experienced profound COVID-19 impacts. Specifically, sites had to maneuver
As the COVID-19 pandemic has forced a shift toward remote modalities, mobile health (mHealth) technologies have been on the rise.
The discussion on decentralized clinical trials (DCTs) has been brought to the forefront in the wake of the COVID-19 pandemic.
We’ve heard and used the term “patient centricity” for years now, and with good reason. It’s an important consideration in
Patient-centric trial design, combined with eConsent, fosters better communication, comprehension, and retention, ensuring a smoother, more informed journey.
Many research and development (R&D) organizations across the industry have limited access to a quality department in the early stages of