SCOPE Europe 2023: Decreasing Burden in Data Collection
In an interview at SCOPE Europe 2023 with Applied Clinical Trials Editor, Andy Studna, Tony Mikulaschek, VP, eCOA, IQVIA Technologies addresses what stakeholders should be thinking of in the data collection space moving forward.
Mikulaschek: DHTs and COAs are really important for the industry, the regulatory bodies have defined the need for that information. For regulatory submissions they are very, very interested in the data from the patient perspective of the therapies and what they do, so it's important that we capture that information. That's one. Number two, we need to make sure that capturing that information is not too much of a burden for the subjects or the sites, so we can make sure that we can continually have the consistency in the compliance to meet the protocol needs without burdening sites or patients.
SCOPE 2024: Todd Everhart of Signant Health Discusses DCTs and Site Burden
February 13th 2024In an interview with ACT editor Andy Studna at SCOPE, Everhart, MD, FACP, clinical vice president, internal medicine, Signant Health discusses decentralized trials and how they may be increasing site burden.
SCOPE 2024: Wendy Morahan of IQVIA Discusses the Use of AI in Clinical Trials
February 13th 2024In an interview with ACT editor Andy Studna at SCOPE, Morahan, senior director, clinical data analytics, IQVIA Technologies discusses how AI can advance trial execution and what stakeholders should be keeping top of mind when choosing technology vendors.
