A brief review of “A Quick Guide to Clinical Trials,” edited by Dr. Madhu Davies and Dr. Faiz Kermain.
May 14, 2008-“A Quick Guide to Clinical Trials,” edited by Dr. Madhu Davies and Dr. Faiz Kermain, and offered by BioPlan Associates, truly lives up to its title. While it could serve as a textbook for a primer class on the clinical trials industry, the quick read would be suitable for anyone wishing to learn more about clinical trials-including people outside or inside the industry. If you are in data management, for example, and want to learn more about ethics in clinical research-or vise versa-this would be a useful resource. The book consists of 14 chapters dedicated to a different segment of the clinical trials process, each written by an industry expert. The information is up-to-date and offers personal, yet professional, insights into the current issues applicable to that segment.
For more information or to purchase, contact: www.bioplanassociates.com/quickGuides.
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.