In the News
ICON experts frequently author or contribute to industry trade press.
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Real-world Evidence and the ‘Unsticking’ of Health Care Data
Ramita Tandon outlines in this article in Managed Care how Pharma and CROs must set high standards for acceptablereal-world evidenceresearch.
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The Future of Clinical Trials
In this article Jennifer Byrne discusses thefuture of clinical trials.
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Preparing for 2026
Vicki Anastasi contributes to this article which looks atvalue-based healthcare, enabled by wearable and electronic health record (EHR) technologies.
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2016 FDA Guidance Documents You Should Know
Gordon MacFarlane, senior manager of regulatory affairs and Cynthia Nolte, director of regulatory affairs outline the key points, benefits, and challenges of theFDA guidance documents during 2016 for medical device manufacturers.
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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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Why Sites Matter
Jennifer Byrne CEO of PMG Research contributes to this article oninvestigative sites and the drug development process.
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Adaptive Designs for Clinical Trials
Read more aboutadaptive design for clinical trialsand how it can improve speed to market.
