Featured Articles
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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.
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Practical Strategies For Diverse Trial Recruitment
11/11/2024
The clock is ticking on the requirement for pharmaceutical companies to include FDA-mandated diversity action plans for pivotal studies in clinical trials.
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Maturity Model For Clinical Trial Disclosure
11/11/2024
Learn about the eight key domains that are assessed by the clinical trial disclosure maturity model.
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Transforming Clinical Trial Disclosure With AI
10/23/2024
Unlock the full potential of AI to address sponsor challenges including regulatory complexity, clinical trial disclosure requirements, and growing demands for transparency.
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AI in Pharma: Benefits, Risks, And The Road Ahead
10/23/2024
How could leveraging AI technologies, including machine learning (ML) and generative AI (GenAI), enable your company to streamline processes from drug discovery to post-launch?
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A Promising Rebound in Clinical Trials
10/23/2024
This report explores how clinical trials bounced back in 2023 from their decline a year earlier despite continued geopolitical, regulatory, and pricing pressures.
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The Importance Of A Maturity Model For Clinical Trial Transparency
10/23/2024
A comprehensive maturity model for clinical trial disclosure and transparency offers companies a strategic tool to assess and enhance their practices in an increasingly complex regulatory environment.