Without the right independent expertise, sponsors launching obesity trials risk misidentifying adverse events (AE) and creating conflicts of interest. Independent experts can provide a more consistent evaluation of AEs, safety, etc. This helps ensure rigorous regulatory submission and eliminates any perception of conflict of interest. The Problem Sponsors with injectable diabetes therapies are now moving […]
Originally posted on MedTech Outlook. Beneficial relationships between companies that begin with trust and shared responsibilities ensure the best business outcomes. A similar, well-grounded partnership evolved when WCG acquired an imaging core lab, Instrinsic Imaging, to expand their suite of clinical services and technologies that maximize the speed and efficiency of clinical trials. The newly branded […]
Watch Knowledge Forum On-Demand About the Knowledge Forum Are you seeking meaningful scientific innovation to support quality data for your schizophrenia trial? Watch this special Knowledge Forum to gain scientific perspectives from pioneers in the Central Nervous System trial world and experts in clinical endpoint solutions: In a decentralizing, peri-pandemic trial world, schizophrenia research has […]
What better way to assess a person’s ability to perform the activities of daily living than to ask them to actually perform those activities? The challenge, of course, is doing that in a controlled, scientifically validated environment. WCG’s Virtual Reality Functional Capacity Assessment Tool (VRFCAT) allows clinicians and researchers to do just that: It assesses […]
About the Webinar We’ve seen significant advances in the use of artificial intelligence (AI) and machine learning computer applications to aid and augment the field of radiology. What is the status of the technology today? How does it receive FDA clearance? In radiology, artificial intelligence applications often require conducting multi-reader multi-case (MRMC) studies on their […]
Choosing Between Provisioned, BYOD, and Hybrid Models for ePRO: Which Is Right for Your Clinical Trial?
As more and more trials opt to include electronic patient reported outcomes (ePRO), sponsors must consider whether they will provision devices or use a bring-your-own-device (BYOD) model. In some cases, they may choose a hybrid option that allows some participants to use BYOD and others to receive provisioned devices. This article explores some key factors […]