The digital options available today reduce patient and investigator site burden, accelerate startup and enrollment timelines, and ensure consistent, high-quality assessments and data collection.
November 17, 2020
An important trend in the dermatology clinical space is the increasing use of technology for virtual visits, remote electronic consent and other applications. With the COVID-19 pandemic as a driver for uptake, teledermatology has gained more widespread use across the world for clinical consultation, patient assessment and follow-up. Virtual visits are of increasing interest in dermatology clinical trials as a way to reduce the study visit burden for both patients and trial sites.
To be most successful, dermatology clinical trials should not only be digitally enabled, but accessible to a diverse array of qualified patients and designed to encourage patient participation. The digital options available today reduce patient and investigator site burden, accelerate startup and enrollment timelines, and ensure consistent, high-quality assessments and data collection.
Join PPD experts Rose Blackburne, MD, MBA, Executive Medical Director, Global Product Development; Norma Cantu, Senior Director, Project Management; and John Manns, Senior Director, Innovation and Digital Operations, for a live webinar on Friday, December 4, 2020 at 10 a.m. EST (3 p.m. GMT/UK).
For more information, or to register for this event, visit Developing a Digital Protocol for Dermatology Trials: A Step-by-Step Guide to Optimizing Research for Patients and Clinicians.
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