Citeline
@Citeline
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Trusted partner of the top 50 global pharmaceutical companies and the top 10 CROs, providing timely intelligence and insight to make authoritative decisions.
Worldwide
Joined June 2010
Matt Holms, Citeline’s VP of Sales, Patient Engagement & Recruitment, emphasizes the importance of collaboration in solving patient recruitment problems. Watch for more on the challenges and opportunities of the current generation of patient recruitment: https://t.co/lv6JjWXmKp
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Explore how CROs are winning contracts in unfamiliar indications: https://t.co/z5LnU6hgP3 With AI-powered analytics, proposals are built faster and backed by evidence sponsors trust. Learn how others are expanding their reach without increasing internal resources.
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🚨 Don’t miss the report everyone is talking about. The Scrip Asia 100 ranks the top 100 pharmaceutical companies in Asia by sales and delivers exclusive insights into the region’s most powerful moves. Download your copy! https://t.co/zk0p7rRqA4
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Webinar alert! Last chance: https://t.co/iMuWpqMznH Pharma teams don’t need more data—they need a unified data picture to make faster, better decisions. This webinar shows how connected data and trustworthy AI optimize protocols, accelerate feasibility and link metrics.
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Your source of truth for clinical trial disclosure: https://t.co/bnKTGIP3e4 Our content ensures full audit readiness with direct links to source materials for added context. Watch #EXTRA2025 sessions featuring forward-looking analysis from clinical trial transparency leaders.
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News is everywhere. But can you trust it? How can you leverage it to gain a competitive edge? Start your free trial: https://t.co/U4l2nHJahF Unlock world-class journalism and analysis of the pharma, biotech, medtech, and consumer health industries with a 1-week free trial.
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Citeline is able to capture data in a way that ensures patient confidentiality and the ability to cross-link through the patient journey. The right data can give sponsors an edge in patient recruitment. Watch the full webinar, Built-In Data Advantage: https://t.co/etz6USXllT
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You bring the questions. We bring 500+ expert voices. https://t.co/dIPYY6VqRm | Discover how Ask the Analyst adds power to your expertise. With Ask the Analyst, Citeline subscribers get direct access to a network of over 500 industry experts in their fields.
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https://t.co/C6eLjHmh3r | In an @endpointsnews article on the potential of neurology assets in biopharma M&As, Citeline analyst Emma Wille comments on how the adoption of AI might speed identification of successful candidates.
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Missed ESMO 2025? Get the insights and analysis in one place: https://t.co/TZylyS7BJ1 The Scrip ESMO 2025 eBook is your essential roundup of the biggest breakthroughs, expert interviews, and commercial impact from this year’s congress in Berlin.
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October 2025 updates: ✔️ Venezuela fee hikes; Belgium’s faster assessments (Jan 2026) ✔️ UK transparency rules (Apr 2026) ✔️ Indonesia registry migration ✔️ ISRCTN registrations during ClinicalTrials[.]gov delays ✔️ ANZCTR prioritization for local trials https://t.co/7oSx7sE9gV
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In a @FiercePharma article on @GSK's Blenrep, senior analyst David Dahan weighs in on @JNJNews's Darzalex, the drug's main contender: https://t.co/FsreK7hkob
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Catch Our on-demand webinar on: Navigating Disclosure Complexity' with RAPS and Citeline experts Brian Kuzich and Jack Marks. | https://t.co/wFlqYg80Bk Ready to revolutionize transparency in pharma and medtech?
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Are you using ‘trustworthy’ AI? Join us to see how unified, high-quality data integrated with trusted AI can transform your protocol optimization, feasibility, forecasting and planning. Register today: https://t.co/uj05ipYVRJ
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Join Ben Evans for a session on the intricate regulatory landscape of clinical trial data disclosure in Asia. https://t.co/QYPB390gQw Navigate through diverse transparency standards, compliance demands and truly transform the way you see global regulatory data disclosure.
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ICH GCP guidelines have changed. Are you prepared? These updates impact everyone running clinical trials—from sponsors to CROs. Our experts break down what’s new and what you need to do next in our on-demand webinar. ✅ Watch now: https://t.co/1PBW4KpoKB
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Asia’s Biopharma Revolution: https://t.co/BxDQjwz7F0 China leads the world in new drug development. Korea and Japan are striking billion-dollar deals. India is stepping into innovation with first-in-class breakthroughs.
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The final webinar in our clinical trial disclosure series spotlights plain language summaries - a growing global requirement that bridges science and patient understanding. Gain actionable insights to strengthen your approach to transparency: https://t.co/uc7LnkFDqx
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https://t.co/OJt14OvjTq | Unleash the future of clinical trials today with Citeline’s new AI Importer, redefining efficiency in protocol registration. This trailblazing tool automatically fills 90+ fields in registration forms, reducing errors and saving you time.
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Pharma teams don’t need more data — they need a unified data picture to make faster, better decisions. This webinar shows how connected data and trustworthy AI optimize protocols, accelerate feasibility and link metrics. Save your spot today: https://t.co/zX8LRvsCg3
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