Insights Blog

The Future of Clinical Research Technology

Posted on Mar 16, 2017 12:15:25 PM

This post is Part 2 in a series based on the Complion webinar,  The Future of the Clinical Research Industry, as presented by John Neal, CEO of PCRS Network. In that webinar, John explores a variety of factors that are driving the evolution of clinical research.

We have the good fortune to live in an age when we are surrounded by technologies that are improving the speed and efficiency with which we can gather information, and the depth and breadth of that information. “In my research I’ve come across dozens of different devices out there that are already being used, some of which are collecting hundreds, and in some cases literally thousands and thousands of data points per second,” John says.

The amount of information being collected presents its own unique challenges, as well as tremendous opportunities for the clinical research industry. John points out that new technologies provide the ability to monitor and collect data when a study volunteer isn’t on site, and with greater accuracy and efficiency than is possible with the diaries used by volunteers. With those diaries,  “the volunteer, the study subject, has to take the time to sit down and record information,” John says. “Let’s face it, in many cases their recall might not be perfect.”

According to John, such manual methods of data collection will be replaced by devices that can accurately calculate, collect, and transmit that data. Such devices “create some tremendous opportunities for us,” John says.

These new methods of data collection are erasing the importance of distance and location in clinical research. As John points out, visits no longer need be conducted at the research site. Data can now be collected remotely without the study subject being at the research site. “We now have the ability as an industry to collect many more data points outside of what’s going on at the site,” John says.

But taking advantage of those opportunities will require overcoming basic human aversion to change. “One of the pushbacks is going to be people simply wanting to hold onto their processes,” John observes. “People are going to hold onto their processes as long as they can.  It’s a job protection issue.”

But the technologies are available, such as Complion’s Document Management solution, and their adoption is inevitable, John believes. “Adoption of electronic records all across the board, consent forms, source docs, diaries, all of those sorts of things will become commonplace in the future and they’re going to facilitate efficiencies in the industry,” he says.

Continue reading the next post: "The Future of Clinical Research: Site Selection"


Access the full on-demand webcast, “Predictions: The Future of Clinical Research,” featuring John Neal, CEO of PCRS Network.

Topics: Clinical Research Trends


Lisa Bozza Archer

Written by Lisa Bozza Archer

As a former Clinical Research Associate with one of the largest CROs, Lisa obtained a strong foundation in clinical research and therapeutic areas ranging from Neurology, Rheumatology, Endocrinology to Oncology. She also gained additional exposure to site operations while working in the Compliance Office of an Academic Medical Center, where she helped support investigators with regulatory and research tasks. These experiences provide her keen insight, both to the needs and the daily experiences of Complion's clients. As an Account Manager of Complion's Customer Success Team, Lisa regularly engages with clients to promote successful adoption and utilization of the Complion System. She actively educates and promotes awareness of Complion’s solution to clients and the research community. She also enthusiastically advocates for sites by leading Complion's initiative to provide free educational webinars to the research community. Lisa shares the Complion team’s intrinsic motivation to reduce the burden on research sites, while increasing efficiency and compliance throughout the industry.

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