Advarra Launches Study Design Solution, Powered by Braid, to Improve Operational Efficiency in Clinical Trials — Read the Press Release

Advarra Blog

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Ways to Streamline Informed Consent Process in Clinical Trial Startup

Optimizing the informed consent process is critical for accelerating clinical trial startup while maintaining compliance and participant understanding. This article explores key strategies for streamlining informed consent, including leveraging electronic consent (eConsent) solutions, standardizing templates, and improving collaboration between sponsors, sites, and IRBs. By implementing these best practices, research teams can enhance efficiency, reduce delays, and improve the participant experience in clinical trials.

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Op-ed: Missing Elements of the Discussion on Decentralized Trials

The discussion on decentralized clinical trials (DCTs) has been brought to the forefront in the…

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Does This Study Require IBC Review?

Gene therapy research is highly regulated due to associated risks, often leading to confusion among…

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4 Questions to Ask When Evaluating Your Research ROI

Key ROI metrics—like publications, staff impact, and core contributions—provide insight into research value and support…

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Sites: The Key to Patient Centricity in Clinical Research

We’ve heard and used the term “patient centricity” for years now, and with good reason.…

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Connecting Patient Centricity and eConsent Together

Patient-centric trial design, combined with eConsent, fosters better communication, comprehension, and retention, ensuring a smoother,…

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Reflections from Cell and Gene Meeting on the Mesa 2021

I recently had the privilege of both presenting at and attending the 2021 Alliance for…

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Implementing a Quality Management System

Many research and development (R&D) organizations across the industry have limited access to a quality department…

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Encouraging Site Centricity and Collaboration at Onsemble

During the week of October 5-8, more than 1,700 Advarra technology customers gathered virtually for…

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Screen Failure in Clinical Trials: Improving Reconciliation

More often than not, researchers face screen failures during the study activation process. Screen failures…

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Leveraging Data to Lead and Manage the Research Mission

Academic research institutions may not face the financial scrutiny of commercial sites, but they still…

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The Importance of Keeping DSMBs Independent

Establishing DSMB independence helps mitigate bias, ensuring clinical trials adhere to regulatory standards and build…

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Beginner’s Guide to Connected Clinical Research Ecosystems

A well-managed, participant-centric clinical trial has many moving parts, and easy access to the right…

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