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Firecrest eConsent, an electronic informed consent solution that incorporates recommendations from the FDA¹s recent draft guidance on informed consent.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Firecrest eConsent, an electronic informed consent solution that incorporates recommendations from the FDA¹s recent draft guidance on informed consent.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.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.