Blog

Advarra acquires Longboat to help advance clinical research and accelerate drug development.

Our experts answered some of the most popular questions from "Racial Diversity in Clinical Trials: Building Trust in Participant Engagement."

Checking the box is still an option on the FWA. At this time, institutions must carefully consider whether it makes sense to check the box.

On October 22, 2020, the FDA's VRBPAC met to discuss the development, authorization, and licensure of vaccines to prevent COVID-19.

Learn how to write effective edit checks in electronic case report forms (eCRFs) to help improve data quality in electronic data capture systems.

Daniel Eisenman answers questions from his latest webinar Study Startup Success for the New Generation of Genetically Engineered Vaccines.

In investigator-initiated trials, an investigator takes on the clinical study as both the sponsor and investigator. Learn more about IITs impact on the clinical research industry.

Learn how to improve project management practices at your clinical research organization and reduce the risk of complications on clinical trials.

New California regulations apply to companies who have information about CA residents regardless of where the company is located. Read more:

Find out more about what to report to whom--and when--in the Q&A blog follow-up to our recent webinar. Read the answers to popular audience questions:

Although we had our fall Onsemble virtually, the community remained focused on advancing clinical research. Read more for event highlights:

Continuing education units (CEUs) are a great way to have a record of your ongoing professional development as required in clinical research.