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Webinar

Your Guide to sIRB Mandates

This webinar offers insights to your pressing questions related to single IRBs and explores the key features of federal sIRB mandates.

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Webinar

Budgeting for Single IRB Review

A practical discussion of budgeting considerations for sIRB review, including strategies for policies around external IRB reliance.

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Blog

Regulatory and Ethical Considerations for eConsent in Research

If any part of your informed consent process involves an electronic component, you’re conducting eConsent.

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4 min. read
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E-Book

Advarra Trend Report: Current State of Trial Opportunity and Selection

Insights into the site selection process and the information sites provide as part of site feasibility questionnaire completion.

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Blog

Enhancing Research Conduct Using eConsent

The Belmont Report established informed consent parameters in 1976, but there are no federal regulations surrounding electronic consent.

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5 min. read
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Blog

5 Questions to Ask Your Sponsor for DCT Implementation

Sponsors are uncertain about how to design a DCT to ensure efficient performance delivery, learn how to set your organization up for success.

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4 min. read
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Webinar

Bridging the Gap: A Standardized Approach to Clinical Trial Document Management

Representatives from the Advarra Site-Sponsor Consortium will discuss a standards-based integration and automation of research technology.

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Blog

Beginner’s Guide to eTMF, eISF, and Regulatory Research Documents

Global & FDA regulations dictate how researchers organize & store trial documents. Learn the basics of eTMF & eISF clinical research tools

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5 min. read
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News

Advarra Launches Cloud-Based Secure Document Exchange to Accelerate Study Startup

Solution provides end-to-end integration and automated, seamless exchange of research documents between sites, sponsors, and CROs

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3 min. read
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Blog

Expanding the Ecosystem to Better Serve You

June 30, 2022

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Blog

A Checklist for Optimizing Clinical Trial Study Startup Activities

This checklist outlines key milestones and considerations for sites and sponsors in the clinical trial study startup process.

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7 min. read
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Blog

The ROI of eRegulatory and eIRB Integration

Learn about the benefits to integrating with technology systems such as email, eIRB, CTMS, and other eReg platforms as you increase ROI.

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4 min. read
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