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Developing and Implementing a Successful eConsent Process
As the industry continues to shift from brick-and-mortar trials to more convenient hybrid formats, eConsent proves to be useful.
4 Reasons Your Institution Needs an eRegulatory System
Using physical binders or an internal shared drive can slow research operations. Implementing an eRegulatory system helps institutions streamline research by transforming key workflows.
Top 10 Educational Resources of 2020
We strive to create meaningful and relevant content for the clinical research community. Check out our top resources of 2020.
Advarra to Bring True Single Sign-On Capabilities to Clinical Trial Sites, Increasing Efficiency and Improving Security
New technology ends swivel-chair effect, reduces friction, frees time to focus on patients COLUMBIA, MD – Advarra, the market leader...
Updated IRB Policies for Research Involving Minors
Advarra has updated its IRB policies for research involving minors. This includes policies on obtaining a child’s assent as well as parental consent requirements.
Evaluating eConsent: Some Considerations from an IRB Perspective
eConsent technology can often better inform participants than just the traditional paper consent, which is great from an IRB perspective.
Generating Leadership Buy-In for a Clinical Research Business Intelligence Solution
Strategies for convincing leadership to invest in the tools needed to optimize operations and inform strategic decision-making.
Patient Recruitment and Enrollment in Clinical Trials
Learn more about patient recruitment and enrollment: how they find out about clinical trials and the reasons they participate.
Clinical Trial Startup: Insights from the Industry
Clinical research professionals provide relevant insights into challenges and barriers impeding study start up.
Q&A from Remote Monitoring: Study Compliance In A Changing World
In a recent webinar, Advarra experts provided insights and information in Remote Monitoring: Study Compliance in a Changing World
Beyond the Regulations: More Considerations for Emergency Research
Go beyond the regulatory requirements and examine three key actions research organizations must consider before conducting planned emergency research.
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC are integral to efficient clinical research. This blog explores how they work together and their differences.
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