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The biosimilar landscape is changing. Recent regulatory developments could streamline development, accelerate market entry and intensify competition for off-patent biologics. In a new PM360 Think Tank article, six indust...

Advancing an asset towards human studies but not there yet? Stop by ICON Booth \#1861 and speak with one of our drug development scientists. Learn how we approach development and how our nonclinical, CMC, and regulatory ...

When a data issue is closed, how do you know it’s really been resolved? Join Shabeeb Kannattikuni at the PHUSE Single Day Event in North Carolina, where he’ll share a SAS-based solution to checking data issue resolution...

Successful obesity trials depend on reaching and engaging the right patients. At #ObesityWeek, visit ICON at booth \#212 to explore recruitment expertise and retention-focused strategies designed to support long-term eng...

Creativity can be a powerful way to connect and understand different perspectives. To recognise Invisible Disabilities Awareness, 62 colleagues came together at our Mexico City office for a watercolour workshop focused ...

Congress participation decisions made easier. Meetings are expensive, arrangements are time consuming. With 50+ data fields to compare details, PubsHub Journals & Congresses makes your decision making faster and easier. ...

The 2028 milestone Orphan medicinal products will come under JCA rules in January 2028, with all remaining medicines following by 2030. For sponsors already in phase 2, the decisions made today could shape future Europea...

Biopsies remain the gold standard in MASH clinical trials, but they are far less common in everyday clinical practice. As more patients are diagnosed and managed using non-invasive tests, the gap between routine care a...

The questions facing healthcare decision-makers are becoming increasingly complex. How do we generate better evidence? Measure outcomes more effectively? Apply AI responsibly? Ensure patient perspectives are reflected? J...

ICON will attend the 19th EBF Open Symposium, taking place from 17–19 November at the Hyatt Regency Barcelona Tower. Join us at booth #B1 to meet our experts and learn how ICON delivers high-quality bioanalytical soluti...

Getting actionable FDA feedback starts long before your submission. A well-prepared Pre-Sub can help AI-enabled SaMD developers clarify requirements, address risks early and make the most of valuable FDA review time. L...

Pharmacovigilance obligations increase once a product enters the market. What worked at launch may no longer scale as products are used in the real world. ICON helps navigate this complexity with post-marketing pharmaco...