Central laboratories are under more pressure than ever. Increasingly complex protocols, frequent amendments, and growing data demands require speed, agility, and uncompromising scientific integrity. At ICON Laboratories,...
In the News
ICON experts frequently author or contribute to industry trade press.
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Moving Beyond a Buzzword: How Small- to Mid-sized Biotechs Can Adopt Patient Centricity in Oncology Trials
A BioCentury article authored by ICON experts Lucy Clossick Thomson, Senior Director of Oncology Project Management & Susan Campbell, Director of Patient Recruitment, discussing how even small steps toward patient engagement can improve cancer trial recruitment and reduce costs.
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America's Best Employers for Women
Read about ICON's recent recognition as a top employer for women in Forbes' 2019 List of America’s Best Employers for Women.
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10 Professionals Predict the Future of Clinical Trials
Discover what the future of clinical trials holds, according to ICON'S Senior Director of Business Development, Sarah Ikard, MBA as recorded by Xtalks in their interview with her at the recent DIA 2019 conference.
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Adoptive Cell Transfer (ACT) Clinical Trials: The Long Road
ICON’s Martin Lachs and Brandon Fletcher provide expert commentary on Adoptive Cell Transfer (ACT) clinical trials in this July 2019 DDN News article.
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Leveraging Novel Therapeutics & Diagnostic Assays
A European Biopharmaceutical Review article featuring expert insights from ICON company MolecularMD's Marissa Pearce on Leveraging Novel Therapeutics & Diagnostic Assays, presenting her argument that, although immunotherapy is nothing new, it has much untapped potential yet to be explored.
This article has been taken from EBR - Summer 2019, Pages. 78-84. Samedan Ltd.
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Technology the Key for Improving Trial Efficiencies & Retention
Past reliance on paper records made for a cumbersome, time-consuming process by making data management highly complex. However, many of the biggest issues remain — in particular, recruitment and retention of patients. Most pharmaceutical companies and contract research organisations have adopted technology solutions, including electronic data capture solutions and clinical trial management systems to increase efficiencies, reduce costs, and improve the patient experience. These solutions have been instrumental in improving clinical trial processes. Read this PharmaVOICE article to learn how the use of technology has become ubiquitous in clinical trials as the industry looks to streamline and improve processes.
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Oncology & ASCO 2019: Moving from Autologous to Allogeneic ACT Paradigms
We have come so far in a relatively short time with Adoptive Cellular Transfer (ACT). ACT approaches have the possibilities of therapies with reduced safety concerns, a higher therapeutic index, as well as breadth of targets including solid tumours. Learn more in our recent Pharmaphorum article.
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The Perverse Incentive: A Unified Approach to Patient Engagement
In operationalising a clinical trial, there are an increasing number of patient facing technologies to aid data collection, enable patient support and improve retention and compliance, with the potential to benefit patients and sponsors alike. Learn more in this recent International Clinical Trials (ICT) article on the need for a unified approach to patient engagement.
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ICON Acquires MeDiNova Research Site in Europe & Africa
This recent Applied Clinical Trials article discusses ICON's acquisition of majority shareholding in MeDiNova Research, a site network with research sites in Europe and Africa, granting our company the right to acquire the remaining shares in the company by the third quarter of 2020. MeDiNova Research currently has a network of 33 active clinical research sites in the UK, Spain, South Africa, Poland and Romania.
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The Digital Trial: How Technology Is Changing Trial Design, Start-Up And Close-Out
The constant data stream from patients’ mobile devices and sensors generate large datasets that are difficult to analyze manually—just one motion sensor gathering data from a few dozen patients creates nearly one billion data points per day (ICON). To understand these large datasets, AI and machine learning are necessary to automate analyses. Incorporating this technology can lead to faster and more transparent access to data. In addition, it can help sponsors collect the right data to support submission and filing for regulatory review, and, in the end, speed a product’s path to approval and reduce time to market. In this Clinical Informatics News article, featuring commentary from ICON expert Marie McCarthy, leveraging technology to accelerate study close-out is further discussed.
