Why Keep HIPAA Separate from the Informed Consent Form
The research informed consent form (ICF) is designed to provide prospective participants with the necessary information to make an informed
The research informed consent form (ICF) is designed to provide prospective participants with the necessary information to make an informed
The pandemic proved decentralized clinical trials (DCTs) can reduce patient burden while delivering quality data in a streamlined environment. In
Optimizing clinical trial access for potential patients is a critical goal for researchers and sponsors. How can we make clinical
A clinical research trial can only be as strong its participant population, but it’s challenging to find eligible patients.
Historically, decentralized clinical trials (DCTs) were heralded as the future of patient-centered research. But how can your organization “walk the
The discussion on decentralized clinical trials (DCTs) has been brought to the forefront in the wake of the COVID-19 pandemic.
Decentralization is one arrow in the quiver to modernize clinical trials.[1] Yet, owing to the varied approaches and possible components