Featured Articles
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The Value Of Continuity: Program-Level DSMBs
4/19/2024
Discover the strategic benefits of deploying consistent Data Safety Monitoring Boards (DSMBs) members across therapeutic programs.
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Implementing eSource: A Guide For Operations And Technology Roles
1/19/2024
By recognizing and addressing the challenges associated with eSource integration, research facilities can fully harness its transformative potential, optimizing efficiency and reliability.
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Why Now Is The Right Time To Adopt eConsent
12/19/2023
As much as eConsent helps staff, participants are also likely to prefer it over traditional paper methods. Explore the benefits of eConsent and some strategic steps sites can take right now to adopt the process.
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NIH 2023 Data Management And Sharing Policy FAQs
12/19/2023
Uncover how the DMS policy intends to promote transparency, collaboration, and the rapid transformation of research outcomes into tangible advancements for the betterment of human health.
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Professional Services Expedite Hospital's Study Process
11/17/2023
Explore the details of a transformative partnership where a children's hospital was able to overcome coverage analysis and budget negotiation issues despite a significant staff turnover.
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Clinical Trial Startup: Insights From The Industry
11/17/2023
Uncover key survey findings gleaned from the perspectives of over 500 clinical researchers regarding technological trends and recommendations for enhancing the overall site experience.
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Global Comprehensive Audit Support
10/26/2023
Uncover how a pharmaceutical company and its strategic partners were able to provide oversight of key performance indicators relevant to the pharma's business model, which enabled escalation and remediation of any concerns.
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Good Manufacturing Practices: When Do They Apply?
10/26/2023
What expectations were set by the FDA regarding the implementation of current Good Manufacturing Practices standards for investigational drugs?
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Study Activation Survey Report Sheds Light On Trials
10/18/2023
Utilize this report to enhance the overall site experience during clinical trial operations, improve site experiences, expedite study initiation, and advance clinical development.
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Navigating CAPA: Ensuring Compliance And Quality Assurance
10/18/2023
For clinical development entities, see how a well-executed CAPA system can function as a guide and steer the course toward continual enhancement while upholding regulatory adherence.