Featured Articles
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Answer Your Critical Clinical Questions — Faster Than Ever
2/19/2025
Pressing clinical planning questions to ask about feasibility, investigator selection, patient enrollment, clinical trial disclosure, and more.
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Antibody-Drug Conjugates: 'Magic Bullets' Become Reality
2/19/2025
Cancer therapy has evolved from potent chemotherapy to targeted biological therapy, including antibody-drug conjugates (ADCs). Learn more about ADCs’ makeup, mechanisms, and the development landscape.
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The Scoop On The SCOPE Summit
2/19/2025
From industry partnerships to patient recruitment to proprietary data, SCOPE 2025 was packed with informational sessions.
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Merits Of A Multifaceted Approach To Clinical Trial Recruitment
1/27/2025
The best way to address clinical trial recruitment challenges is with a multifaceted approach that goes beyond traditional channels and ways of thinking.
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Use Case: A Patient-Centric Approach To Site Selection
1/27/2025
Discover how Citeline’s robust datasets, combined with real-world data, inform intelligent site and investigator selection for a rare, autoimmune disease.
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What's The Current & Future Impact Of AI On Pharmaceutical R&D
1/17/2025
Explore the results of a survey where senior decision-makers in the life sciences industry provided their perceptions and expectations of AI to understand current AI adoption trends.
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What Does 2025 Hold For Pharma?
1/17/2025
Look at what’s in store for pharma and life science in 2025. While we see many recurring themes, 2025 promises to be filled with unexpected — and possibly unprecedented — developments.
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Top 10 Tips For Diversity Plans
12/13/2024
Explore the updated guidance from the FDA to enhance diversity in clinical trials, including ten times to developing a comprehensive Diversity Action Plans.
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Artificial Intelligence Regulation
12/13/2024
To make the best use of artificial intelligence (AI), drug sponsors need to understand where health authorities are drawing the lines.
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Ensuring A Diverse Patient Population In Clinical Trials
12/13/2024
In 2025, the FDA will require pharmaceutical companies to include diversity action plans (DAPs) for Phase II and pivotal studies.