Insights On Partnering
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Tech Transfer Strategies For mAb Drug Products In Late-Phase Launch
8/7/2025
Tech transfer is not just a process of replicating manufacturing steps; it is a complex, multidisciplinary effort that ensures process robustness, scalability, regulatory compliance, and supply chain readiness.
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Central eSource Is The Latest In Sponsor Provided Site Offerings
7/7/2025
For decades, sponsors have provided tools to help clinical sites work more efficiently. Central eSource is the latest evolution in this trend.
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Elevating The Site Voice
3/27/2025
A decentralized trial can be daunting for sites, but Medidata offers solutions to help site staff, sponsors, and patients move smoothly through the clinical trial process.
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Why Biotech CRO Partnerships Are Essential For Clinical Trial Success
5/29/2025
For early-stage biotech companies, the road from discovery to market is fraught with challenges, and in this environment, strategic partnerships with CROs have become a cornerstone of clinical success.
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Medable's Japanese Clinical Trial Exceeds FPI Date And eCOA Adherence
3/10/2025
A top-10 global pharma company aimed to address eCOA adherence and patient enrollment challenges faced by clinical trial sites in Japan. Explore an initiative to enhance the patient and site experience.
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Built Like A Tech Company: Why CROs Need A New Operating System
10/20/2025
See why building digital, automated infrastructure is essential, and better aligns CROs with today's speed, compliance, and innovation needs.
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Optimizing EDC Strategy And Data Collection for a Rare Disease Trial
6/11/2025
Explore how Veristat created a forward-looking roadmap for EDC and CRFs integration for a small biotech sponsor, ensuring a future-ready data ecosystem without overcomplicating current operations.
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Site Management Support To Investigational Sites
9/17/2025
Rare disease trials demand specialized site support. Explore how tailored site management practices can improve consistency, data quality, and patient engagement in complex clinical studies.
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Cutting-Edge Tech Improving Global Participant Payment Paradigms
12/13/2024
Participant payment management is essential for successful global clinical trials, as it enables diverse regulatory compliance, enhances participant satisfaction, and streamlines execution.
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How Site And Patient Research Optimizes Clinical Trials
6/17/2024
Signant’s patient and site research enhances digital health technology in clinical trials by optimizing usability and design. These insights drive improvements in product features, study designs, and training materials.