Supporting Patient-centric and De-Centralized Clinical Trials

By Noah Cotes, Project Manager at Veracity Logic, LLC   Patient-centric clinical trials, also referred to as de-centralized clinical trials are often discussed in the pharmaceutical industry today. To be “Patient-centric” is to reevaluate the needs and realities of the patient experience, and to allow that understanding to inform your clinical trial all the way …

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Why Flexibility is Important in Clinical Trials Supply — and how a nimble IRT partner can help keep your trial on track.

By Andi DeStefano, Director of Project Management at Veracity Logic, LLC. To see why flexibility is important to keeping a clinical trial on track, let’s explore the Clinical Trial Supply Lifecycle using a fictional Sponsor named Pharzm, who will be running Phase 3 trials for a new drug. Pharzm has a new two-year trial, which …

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Choosing an IRT Partner to Extend Your Team’s Resources

Increasing demand for speed while achieving quality results has made partnerships an essential component of today’s clinical trial environment. An ideal Interactive Response Technology (IRT) partner will make the complex processes of subject and inventory management simpler and easier to manage, saving your project team and clinicians time so they can focus on your study. …

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Multiple Randomizations in Clinical Trials

FAQs you can use randomization clinical trials

This is the first of our on-going FAQ series on IRT services in Clinical Trials. You can listen to the recording or read the text below. In April 2020, a client asked: Can your system handle multiple randomizations for a subject at different points during a study? That is, can the subject be randomized to …

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What is a Clinical IRT?

The Basics: IRT stands for Interactive Response Technology; it uses the web or phone to allow users to interact with a system. A Clinical IRT is a web-based tool for managing subjects and inventory during a clinical trial/study. It allows the clinical research site users (including Primary Investigators, Sub-Investigators, and Study Coordinators) to: add subjects to …

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