5 Reasons to Use ePRO in your next Clinical Trial

Approximately 30% of clinical trials use Patient Reported Outcomes* (PRO) as primary or secondary endpoints. PRO can be collected using questionnaires, instruments, diaries, or surveys. The use of digitized PROs, or ePRO (electronic patient-reported outcomes), is on the rise in today’s health research settings for many reasons, including: Studies show that electronic patient reporting yields …

Read more

5 Ways Veracity Logic Can Help Your Next Study Run Smoother

Can Veracity Logic’s IRT system help your next clinical trial run faster and more efficiently?   Yes!  Here’s how:  1) Reduces start up time  Our system is designed to expedite clinical trials – it’s modular and quick to configure, so we can meet tight deployment timelines. The VLIRT system is easy to learn and use, …

Read more

Effective IRT Startup Meetings – Tips for Sponsors and CROs

An IRT (Interactive Response Technology) is the tool of choice for clinical trial subject randomization and management, drug assignment and inventory management, and shipping. The IRT system is often the first point of entry for subject data that is then typically pushed to the EDC housing the clinical database. So when it’s time to hold …

Read more

Are you trading performance for connectivity convenience?

One of the challenges of using software from multiple vendors to support a clinical trial is connectivity. Is minimizing the number of clinical trial vendors the answer? While it can make things simpler for vendor managers, it may come at the cost of reduced performance. Some parts of the system may work well, but some …

Read more

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

OCT Southeast Conference

We’ll be exhibiting at the Outsourcing Clinical Trials Southeast Conference on March 30 and 31st. Visit our booth for a chance to win $100 for the charity of your choice!* For more information, and to register for this virtual event, please go to www.arena-international.com/oct-southeast.  Team news: Andi DeStefano, Veracity Logic’s Director of Project Management, will …

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