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Blog

Our OnCore CTMS Vision: Building a Foundation for Success

More than two decades ago, we created OnCore CTMS. What do we have in store for the future?

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5 min. read
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Infographic

Turbocharging Clinical Trial Activation Timelines

Understanding roadblocks to study activation and what your organization can do to mitigate them can ease study startup burdens.

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White Paper

Operationalizing Research Analytics: Today, Tomorrow, Someday

Uncover how analytics, artificial intelligence, and machine learning are reshaping the foundational elements of clinical research.

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Blog

A Phased Approach to QMS

A phased approach to quality management systems (QMS) ensures quality is embedded at every stage, from discovery to post study.

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3 min. read
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Blog

Thinking About the Box: Considerations for Transport of Investigational Products

Ensure safe transport of investigational products with meticulous planning and rigorous procedures to mitigate hazards and uphold biosafety.

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4 min. read
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Blog

Clinical Trial Startup: Insights from the Industry

Clinical research professionals provide relevant insights into challenges and barriers impeding study start up.

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4 min. read
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Blog

The Role of Financial Management and GAAP in Clinical Research

Learn how robust financial practices and a CTMS aligned with GAAP principles can drive sustainable growth and efficiency within an organization.

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3 min. read
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E-Book

Unlocking Study Activation: 2023 Study Activation Report

Access the survey report now for current perspectives on study startup activities impacted by rapidly evolving technology and tools.

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Webinar

What Happens When a Study Fails to Meet Its Recruitment Targets?

Explore IRB considerations for overcoming study enrollment barriers while ensuring risks to participants are appropriately minimized.

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Webinar

Best Practices for IRB Review of DCTs: Expert Perspectives

Leverage best practices for IRB review of decentralized trial elements sourced from research community experts.

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Blog

Enhancing Research Ethics: Understanding HRPP Staffing and the sIRB Mandate

Understand the significance of HRPP staffing despite an sIRB mandate, and how HRPP staffing maintains ethical research practices.

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3 min. read
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Blog

GxP Best Practices for Safer, Smarter, Faster Clinical Research

Uncover key regulations and insights regarding GxP in pharmaceuticals, medical devices, and clinical research.

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6 min. read
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