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ICON experts frequently author or contribute to industry trade press.
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Narratives for a clinical study report: The evolution of automation and artificial intelligence
In this article (page 28), find out what the future holds for narrative production in clinical studies now that we are in the era of AI.
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Keeping eCOAs off the critical path – key considerations
The prevalence of decentralised clinical trials and the importance of patient-centricity in medical practices are just two of many factors leading to the increased use of electronic Clinical Outcome Assessments (eCOAs). Digital devices like smartphones, tablets, wearables and web-based platforms are increasingly being used to measure the impact of a disease and/or treatment on patients’ quality of life and are an important way we can capture the patient’s voice in a clinical trial.
The eCOA system consists of the devices used for data collection, specialised eCOA software installed in these devices for collecting the data or access to web-based eCOA platforms and a centralised database or server to store, manage and analyse the data securely. This article explains how an optimised eCOA implementation strategy can minimise several risks and challenges associated with clinical trials.
Article published in International Pharmaceutical Industry, Volume 15 Issue 3, 29 September 2023
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Modern partnerships with CROs
In this article in Contract Pharma, ICON SMEs share insight on strategic and blended outsourcing models and trends in today’s market.
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Driving progress in reducing kit wastage
In this article from European Pharmaceutical Manufacturer,Leonard Wee, VP, Global Supply Chain, Laboratories, explores how shifting to more reliable kit forecasting, in tandem with efficient kit building practices, can help reduce waste, cost and logistical requirements.
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Integration of AI in imaging clinical trials
In this article from Drug Discovery World, Sophie Winandy, Executive Director of Medical Imaging, explores the benefits of AI and how it can be integrated throughout medical imaging within clinical trials.
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Logistical considerations in mRNA vaccine development
In this article, ICON’s Andreas Dreps and Martin Lachs discuss the logistical considerations in mRNA vaccine development.
©BioPharm International
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Considerations for safety data migration methods
In this article, Graeme Bones, Director of Pharmacovigilance, explains how to handle the different types of data migration methods and how companies can select the optimum approach to ensure data integrity is maintained.
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Beyond the glass: A look at digital pathology’s practical applications and novel possibilities in clinical trials
In this article from Diagnostics World News, Jenny Ross, Pathologist and Medical Director, looks at practical uses of digital pathology technologies and illustrates considerations for their use in global clinical trials.
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AI In Clinical Research: Now And Beyond
In this piece from Forbes, Dr. Greg Licholai, Chief Medical and Chief Innovation Officer talks about recent developments, regulatory considerations, and the promising future of AI in clinical research are reshaping the landscape of drug development and patient care.
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ICON interview: Insights on the new EMA guidelines for computerised systems and electronic data in clinical trials
Outsourcing Pharma spoke to Vesta Marciulioniene, director global regulatory clinical services at ICON Biotech, who shares her insights on the new EMA guideline for computerised systems and electronic data in clinical trials and what new expectations it sets for the clinical research industry.