Beginner’s Guide to Medicare Coverage Analysis
Medicare coverage analysis offers clinical sites a clear billing framework, protecting participants and minimizing...
FEATURED E-BOOK
Making Good Clinical Practice More Understandable
This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.
Developing and Implementing a Successful eConsent Process
eConsent simplifies the consenting process for research staff and participants, improving quality and reducing...
Privacy Regulations Impact on Global Clinical Trial Endpoint Adjudication
New privacy regulations seem to form every few months, especially with individual U.S. states...
Why Now is the Right Time to Adopt eConsent
eConsent streamlines trial participation, allowing remote access and minimizing paperwork errors, benefitting both research...
Beginner’s Guide to Budget Negotiation
Effective negotiation balances firm priorities with flexibility, helping sites align sponsor budgets with true...
Beginner’s Guide to Single IRB Mandates
As clinical trial efficiencies grow, understanding single IRB mandates becomes crucial for sites and...
Advancing Diversity, Equity, and Inclusion in Clinical Research: A Path Towards Health Equity
In clinical research, diversity, equity, and inclusion (DEI) is becoming increasingly recognized as...
Your Guide to sIRB Mandates
In the past few years, new regulations and policies have been announced and implemented...
Why Keep HIPAA Separate from the Informed Consent Form
The research informed consent form (ICF) is designed to provide prospective participants with the...
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