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Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

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Webinar

Is Your Site Ready for an FDA Inspection?

Understand the FDA’s expectations for a site inspection, GCP compliance, and maintaining study integrity.

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E-Book

Trend Report: 2023 Trends Impacting Clinical Research

This report defines 2023 clinical research trends and provides an outlook for the industry moving forward.

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Blog

How Paper and Electronic Source Data Meet ALCOA-C Principles

ALCOA ensures source data is safe and effective, but how does it differ for data collected on paper vs. electronically?

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3 min. read
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Webinar

Inspection Readiness: Before. During. After

This webinar will cover successful strategies for a proactive approach to FDA inspections before, during, and after.

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Blog

Beginner’s Guide to 21 CFR Part 11 Compliance

FDA released regulations in 1997 outlining how 21 CFR Part 11 applies to electronic records and electronic signatures in clinical research.

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4 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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Podcast

AI in Clinical Research

In this episode, we explore the ethics and implications of artificial intelligence in clinical research.

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Blog

Q&A: Stepwise Implementation of a Clinical Quality Management System

Advarra expert Steffen Engel answers questions from the webinar, Stepwise Implementation of a Clinical Quality Management System.

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8 min. read
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Case Study

Advarra Consulting Delivers Clinical Trial Management Oversight

Download this case study to learn how Advarra Consulting mitigated risks and enabled compliance for a medical device organization.

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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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