Long-term follow-up for vaccines may seem to be a distant concern when clinical trials are just beginning, but it can be critical to have a plan for follow-up at the outset. Learn considerations for follow-up design, s...
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ICON experts frequently author or contribute to industry trade press.
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One Answer to Your Postmarket Challenge: Planning
Interview with Vicki Anastasi onpostmarket surveillance and the challenges trial designs are facing.
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The Clinical Trial of the Future
Steve Cutler talks to Pharma Times regarding industry trends inclinical trials and patient engagement.
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Match This
Due to considerable market growth, biosimilar clinical trials are rising in popularity. One key example relates to rituximab, and the development of its biosimilars is currently leading the way in clinical research.
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Remote Monitoring of Patients in Clinical Trials
Recent initiatives to redesign theclinical trial processhave in part focused on the creation of trials that are more patient focused.
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Adaptive Designs for Clinical Trials
Read more aboutadaptive design for clinical trialsand how it can improve speed to market.
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Adaptive designs patient value
Vicki Anastasi contributes to this article that looks at adaptive designs patient value and commercial benefits.
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The Patient Data Gold Rush
Tom O'Leary's presentation to the Financial Times Digital Health Summit Europe is covered in this article regarding the use of technology tomine the clinical data patient.
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Bring Your Own Device for Trial Outcome Assessment
A research survey to identify and assess the perceived barriers and challenges with the use ofBYOD for eCOA in clinical trials.
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Countermeasures to Oncology Trial Failure: 5 Smarter Approaches to Trial Design and Analysis
5 Smarter Approaches to Trial Design and Analysis
Alan Phillips, Vice President, Biostatistics and Jia Ma, Senior Program Manager, Biostatistics, of ICON Clinical Research contribute to this article onCountermeasures to Oncology TrialFailures.
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CRO Industry Update
Just as drug products have become increasingly complex, regulatory and payer demands have added a myriad of complexities and costs todrug development.