ICON Launches Electronic Informed Consent
ICON has announced Firecrest eConsent, an electronic informed consent solution that incorporates recommendations from the FDA¹s recent draft guidance on informed consent.
ICON has announced Firecrest eConsent, an electronic informed consent solution that incorporates recommendations from the FDA¹s recent draft guidance on informed consent.
The e-Consent solution is a component of ICON¹s new informatics hub designed to enhance the engagement of patient populations in the drug development process. The solution employs videos and visual aids to assist in the explanation of complex scientific concepts and medical terms found in trial protocols.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Phase III PROMINENT Trial Initiated to Evaluate Felzartamab for Primary Membranous Nephropathy
June 30th 2025The global Phase III PROMINENT trial has begun dosing patients to evaluate felzartamab in treating primary membranous nephropathy, a serious autoimmune kidney disorder with no FDA-approved therapies.
Funding Cuts Threaten Diversity in Clinical Research
June 27th 2025In this video interview, Kyle McAllister, co-founder, CEO, Trially, discusses how recent federal funding cuts are likely to undermine research focused on underrepresented populations, and why long-term investment in community-based studies is essential to closing persistent health equity gaps.
