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Category - Any - Industry Webinars Workshop Industry CTO West Coast Date 28 April 2026 - 29 April 2026 Time 08:00 - 18:00 Location San Francisco, CA, USA Timezone America/Los Angeles ICON will exhibit and speak | Booth #2 Industry Bio Korea Date 29 April 2026 - 30 April 2026 Time 08:00 - 18:00 Location Seoul, South Korea Timezone Asia/Tokyo ICON will exhibit | Booth #G25 Industry SCDM EMEA Date 3 May 2026 - 6 May 2026 Time 08:00 - 18:00 Location Copenhagen, Denmark Timezone Europe/Copenhagen ICON will exhibit and speak | Booth #11 Industry RAPS Euro Convergence Date 5 May 2026 - 8 May 2026 Time 08:00 - 18:00 Location Lisbon, Portugal Timezone Europe/Lisbon ICON will exhibit | Booth #21 Industry OCT Europe Date 6 May 2026 - 7 May 2026 Time 08:00 - 18:00 Location Barcelona, Spain Timezone Europe/Madrid CON will exhibit and speak Booth #52 Industry AAPS NBC Date 11 May 2026 - 14 May 2026 Time 08:00 - 18:00 Location San Diego, CA, USA Timezone America/Los Angeles ICON will exhibit | Booth #404 Industry OCT East Coast Date 12 May 2026 - 13 May 2026 Time 08:00 - 18:00 Location New Brunswick, NJ, USA Timezone America/New York ICON will exhibit and speak | Booth #25 Industry DIA China Date 13 May 2026 - 16 May 2026 Time 08:00 - 18:00 Location Shanghai, China Timezone Asia/Hong Kong ICON will exhibit and speak | Booth #K23 Industry ISPOR US Date 17 May 2026 - 20 May 2026 Time 08:00 - 18:00 Location Philadelphia, PA, USA Timezone America/New York ICON will exhibit | Booth #1017 1 2 3 … 5 Next In this section In this section Press releases In the News Mediakit Facts and figures ICON spokespeople Awards Events Industry events ASCO 2026 Webinars Workshops Webinars Social media Connect with us Contact us Submit proposal request Update Email Preferences Global office locator ICON on social media Related information: Solutions Webinars Solutions Industry events Solutions Workshops What's happening in ICON ICON Plc ICON is excited to sponsor RAPS Euro Convergence 2026, taking place 5–8 May in Lisbon. ICON are joining regulatory leaders at RAPS Euro Convergence 2026, taking place 5–8 May in Lisbon. Drop by and meet Gabriel Bohl a... 21 Apr View post View webpage ICON Plc Pediatric trials face unique complexity but selecting a fit for purpose HRQoL measure doesn’t have to. The FDA’s PFDD Guidance emphasizes that historical use is not justification. Sponsors must demonstrate why an instrum... 20 Apr View post View webpage ICON Plc Join us on 6 May at OCT Europe in Barcelona. At 12:00pm in Stream C, Ankita Minhas will present “The global biotech sector: A CRO perspective”. Discover how rising scientific and operational complexity, AI‑driven innovat... 20 Apr 8 View post View webpage ICON Plc ICON Biotech will participate in #CTOWC26, the 13th Annual Clinical Trials in Oncology West Coast, taking place on 28–29 April 2026 in Burlingame, California. The event brings together oncology and clinical research pr... 17 Apr 3 View post View webpage ICON Plc The RACE Act changed pediatric oncology in the US. The EMA’s proposed MoA PIP requirements could do the same in Europe. So what does this mean for sponsors? ICON’s Regulatory Affairs (Graham Bell) and Pediatrics (Jacqu... 16 Apr View post View webpage ICON Plc Proposed requirements for Mechanism of Action based PIPs are coming. Right now, they’re still developing. ICON can help sponsors position to stay ahead of the curve and benefit from incentives while meeting pediatric obl... 16 Apr 1 View post View webpage ICON Plc ICON will participate in BIO Korea 2026 from 28 to 30 April in Seoul, South Korea. The event brings together leaders in biotechnology and healthcare to discuss scientific innovation and industry collaboration. Visit ICO... 16 Apr View post View webpage ICON Plc Strong engagement, open dialogue, and a shared focus on the future. Last week, ICON CEO, Barry Balfe, connected with teams in our São Paulo and Mexico City offices, hosting a series of highly engaged town halls. The vis... 15 Apr View post ICON Plc Patient safety and data integrity are the primary concerns in early phase clinical trials. In the US sponsors generally follow one of two standards sets when conducting early phase trials: Good Manufacturing Practice (GM... 15 Apr View post View webpage ICON Plc In 2025, the EMA and FDA each released regulatory guidance that impacts the development and approval processes for biosimilars, such as by waiving the need for comparative clinical efficacy studies in some circumstances.... 15 Apr 1 View post View webpage ICON Plc Clinical research is evolving at pace and so is the role of the Clinical Research Associate. From increased use of technology and data, to more strategic site partnerships, today’s CRA plays a critical role in deliverin... 14 Apr View post View webpage ICON Plc On 15 April at 12:00 pm, join ICON’s Alan Baldridge at the GLP-1-Based Therapeutics Summit for his session, “Is there anything GLP‑1s can’t do? Unlocking the next generation of metabolic treatments.” He will offer a fo... 14 Apr View post View webpage
