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Blog

Informed Consent: When, Why, and How It’s Obtained

Aside from being a regulatory and ethical requirement, informed consent is a good way to ensure participant knowledge and develop a foundation trust between researcher and participant.

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4 min. read
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Case Study

Helping to Ensure the Success of a Phase III Vaccine Trial

January 24, 2021

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Blog

Understanding the Complexity and Uniqueness of Phase I Trials

There are many distinctions that set Phase I trials apart from the rest. For sites aiming for a successful Phase I trial, working with an organization that understands the nuances is key.

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3 min. read
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E-Book

A Guide to System Integrations and Single Sign-On for Clinical Operations Teams

The growing complexity of clinical trials is being met with a new generation of eClinical tools – electronic data capture, centralized trial platforms, and risk-based management tools.

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Case Study

Meeting Multiple Challenges for a Uniquely Challenging Trial

December 18, 2020

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Case Study

Demonstrating the Impact of the Longboat Portal on Recruitment Success

December 7, 2020

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Blog

The Many Faces of “Coercion” and “Undue Influence”

Coercion and undue influence in research can be complicated. Understand what these terms mean and how to appropriately protect against them.

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5 min. read
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Blog

Takeaways From the FDA’s VRBPAC Meeting – October 22, 2020

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

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Blog

Beginner’s Guide to Investigator-Initiated Trials

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.

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5 min. read
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Blog

Is GDPR Coming to the US? CCPA and Its Impact on Research

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

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Blog

Q&A – The New Urgency of Clinical Trials: How Oncology Leads the Evolution

How has the COVID-19 pandemic changed oncology research--and research in general? Read more for the follow-up blog to our recent symposium:

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Blog

Getting “Engaged” in the Time of COVID

When using remote sites to perform clinical trial procedures, keep in mind things like whether remote sites are considered "engaged" in research. Read more:

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5 min. read
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