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Informed Consent Development Service

Ensure your clinical trial documentation is compliant while making study activation more efficient.

Video

By the Numbers: Our Response to COVID-19

December 18, 2020

We are honored to support a resilient research community during the COVID-19 pandemic. Explore our resources to find out how we keep research moving forward.

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Protocol Calendars

Improve protocol compliance and quality and reduce study activation times by downloading centrally built protocol calendars into your CTMS.

Blog

Standardization and the Importance of Medical Coding Dictionaries in Clinical Trials

December 7, 2020

Learn more about the importance of medical coding dictionaries, their common uses, and best practices.

Blog

The Opioid Crisis in America

July 24, 2020

Combating the opioid crisis requires urgent, evidence-based approaches that address clinical, research, and education issues. Read more:

News

Falcon Consulting Announces Name Change to Advarra Consulting

March 29, 2018

Malvern, PA, March 29, 2018 – Falcon Consulting Group, Inc., a leading global research quality and compliance company, has changed its name to Advarra Consulting, Inc. The new name reflects the organization’s presence as a wholly owned subsidiary of Advarra, Inc.

Webinar

Simple Ways to Uncover Research Compliance Blind Spots

This webinar offers three strategies to check and reduce blind spots regularly to improve compliance oversight.

Webinar

The Must-Haves of FDA and Common Rule Reporting Requirements

The Food and Drug Administration (FDA) regulations governing Investigational New Drug (IND) applications contain specific reporting requirements. Similarly, the Common Rule (i.e., the federal policy for the protection of human subjects) also contains reporting requirements. Of course, the Common Rule and FDA reporting requirements differ. It’s important to understand what must be reported to whom, and that everything is reported within the appropriate timeframe. How can investigators, institutions, IRBs, and sponsors properly manage these responsibilities?

White Paper

GxP Compliance in Clinical Research

November 7, 2023

This white paper walks through key GxP principles and regulatory requirements and gives a real-world case study.

News

How-To Videos Provide Quick, Straightforward Help with Common CIRBI Activities

February 19, 2019

Short how-to videos are now available to assist users with common features and capabilities of the Advarra Center for IRB Intelligence (CIRBI) Platform.

News

Advarra Launches Partner Network to Extend Research Capabilities and Enable Site-Centric Connectivity Across the Industry

May 17, 2022

The Advarra Partner Network fosters innovation at scale through API, Data, and Strategic partnerships, implementing an open, standardized framework to...

Blog

Diversity in Cancer Research: Getting Started

February 16, 2022

Learn how to start ensuring the membership and leadership of your NCI-designated cancer center reflect the population you serve.