A Process for Successful Mid-study Changes

changes in clinical trials can be challenging

Change is a constant challenge in the world of clinical studies, and it can cause both stress and delays. In our last blog, we discussed 5 tips for more effective mid-study changes. Now let’s look at the components of a successful management process for a technical change from an IRT perspective. The IRT Project Manager …

Read more

Five Tips for Minimizing Mid-study Change Delays

Changes

According to a recent survey, managing mid-study changes and their associated delays topped the list of challenges faced while conducting a clinical trial. But there are ways to minimize the impact of mid-study changes. “There are five components to any successful system change,” says David Goldston, President of Veracity Logic. “And thinking through them will …

Read more

Managing Drug Returns with your IRT

Drug accountability is important to gathering quality data as well as for insuring patient safety. The problems associated with it remain key issues for clinical trial management in 2021. Using an IRT (IVR/IWR) system to manage the distribution and assignment of an investigational product (IP) is now a well-established practice. Most IRTs include some method …

Read more

Intuitive Subject Management Systems

Intuitive and user friendly To be effective, an e-clinical solution must be intuitive for all users. For a clinical system to be user-friendly, it needs to be flexible. As clinical trials move more towards virtual environments, it is extremely important to have views of subject data and information that fit the needs of everyone involved …

Read more

Choosing Your IRT Partner for Clinical Trials in 2021

Will you be looking for a new Clinical IRT Partner in 2021? Check out our vendor selection guide! Developed especially for Sponsors, CROs, and Clinical Suppliers, it lists the capabilities and issues to consider when vetting IRT vendors and systems in an easy to use format. We hope you’ll find it useful.   Download your …

Read more

Putting Clinical Study Control Where It Belongs

By Noah Cotes, Project Manager at Veracity Logic, LLC   In the fast-paced world of clinical trials, a lack of information and ability to adapt will leave you in the dust. To address this,  Veracity Logic advocates a “study-team-centric” model of clinical trial execution, where our system facilitates putting the study team in control. To …

Read more

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 …

Read more

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 …

Read more

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. …

Read more