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Webinar

Advantages and Considerations for an eRegulatory Implementation

Gain an understanding of what an eReg system is and the features available to streamline clinical trial regulatory management.

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Blog

4 Unique Challenges of Oncology Trials

Oncology research is unique in many ways, including the challenges researchers face in conducting cutting-edge trials.

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Blog

Improving Study Activation Time for Gene Therapy Research

With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts

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Blog

What Sponsors Need to Know About Medicare Coverage Analysis

Discover the role of MCA in clinical research, its impact on study activation timelines, and how outsourcing can streamline trials.

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3 min. read
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White Paper

4 Modernized Functions Every Sponsor Needs for Study Startup

This white paper outlines four technology capabilities sponsors need to expedite the study startup process.

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Blog

Collaborating with Research Sites: Best Practices for Site Selection and Study Startup

Key strategies for successful research study startup: site selection, documentation, and effective initiation.

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4 min. read
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Webinar

Reducing Site Burden Throughout Study Startup

Learn strategies to streamline workflows across sites and sponsors, and explore success stories on how to reduce site burden.

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Blog

How Single IRB Review Mandates Help Research Sponsors

The proposed single IRB mandates will impact FDA-regulated research, potentially altering existing practices at organizations.

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4 min. read
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White Paper

Unique First-in-Human Phase I IRB Considerations you Might not Know About

An institutional review board (IRB) may ask some different questions for first-in-human (FIH) Phase I trials than later phase studies.

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Webinar

Strategies for End-user Adoption

Learn about potential solutions to help you create new adoption strategies, materials, and build training to optimize end-user acceptance.

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Webinar

Is Your Site Ready for an FDA Inspection?

Understand the FDA’s expectations for a site inspection, GCP compliance, and maintaining study integrity.

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E-Book

Trend Report: 2023 Trends Impacting Clinical Research

This report defines 2023 clinical research trends and provides an outlook for the industry moving forward.

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