Industry Insights
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From Insights To Action: The Transformative Power Of Visualization In Clinical Science
8/11/2025
Explore the critical role of data visualization in clinical research and address the challenges of interpreting fragmented raw data to derive actionable insights that enhance patient outcomes.
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The Rise Of Targeted Modalities In Pharmaceutical Development
8/11/2025
Targeted modalities are pushing the boundaries of technology and therapeutic effectiveness. Their potential to transform patient care depends on leveraging the right expertise, technologies, and partnerships.
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Targeted Protein Degraders: Transforming Oral Therapeutics
8/11/2025
CDMOs play a critical role in TPD development by offering specialized infrastructure and analytical capabilities to support the transition from preclinical research to clinical supply and commercialization.
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Targeted Modalities: Trends, Challenges, CDMO Considerations
8/11/2025
Targeted modalities are designed to bind specifically to receptors or biological targets, ensuring a more directed and effective treatment while reducing systemic exposure and unintended side-effects.
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Future Predictions For Clinical Technologies
8/11/2025
In 2025, sponsors are prioritizing configurable, interoperable solutions that integrate seamlessly across IRT, eCOA, CTMS, eConsent, and supply chain systems.
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A Guide To Electronic Data Capture (EDC)
8/11/2025
EDC systems are designed to support a wide range of clinical research while ensuring compliance with global regulatory standards, revolutionizing data management in clinical trials.
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How To Improve Patient Outcomes Using eSource Software In Clinical Trials
8/11/2025
As the demand for patient-centric clinical trials grows, eSource platforms will play an increasingly vital role in facilitating efficient, compliant, and innovative research methodologies.
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Running Global Clinical Trials? PolyPid Shares Operational And Regulatory Insights
8/11/2025
PolyPid shares its clinical trial journey across the U.S., Europe, and Israel, highlighting operational complexities, regulatory navigation, and the adaptability required to execute large-scale, global studies.
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AI In Clinical Trials: Key Insights From Industry Experts
8/8/2025
Find out what experts from the FDA are saying about AI’s ability to demonstrably impact three critical success metrics in clinical trials.
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How Strategic LQPPV Outsourcing Future-Proofs PV Compliance In The AI Era
8/8/2025
As health authorities seek standardization across global processes and strong AI governance, working with an experienced PV partner will help minimize the burden of oversight and ensure compliance.