Understanding Various Decentralized Terms in Research
As many research organizations are becoming more patient-centric and adapting to technological advancements and remote requirements, they are re-designing the
As many research organizations are becoming more patient-centric and adapting to technological advancements and remote requirements, they are re-designing the
Effective billing compliance starts with understanding routine costs, extended coverage, and administrative fees to avoid costly errors in clinical trials.
The COVID-19 pandemic highlighted the importance of robust emergency preparedness for HRPPs, ensuring research continuity and participant protection during crises.
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.
The year 2021 brought many advancements in the clinical research industry. We’ve pushed for more diversity and inclusion in clinical
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.