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Webinar

Inside Study Activation: Budgeting Takeaways

Upcoming: April 18

Learn how sites, sponsors, and CROs can work together to help study activation, specifically within budgeting and contracting.

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Webinar

Striking the Balance: Ethics, Inclusion, and Vulnerability in Research

Upcoming: April 2

Explore the ethical tensions between including under-represented communities and ensuring vulnerable participant populations are appropriately protected.

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White Paper

sIRB Review for Multicenter Research: A Guide for Institutions

February 15, 2024

Single IRB (sIRB) review for multicenter research is fast becoming the norm in the US. Initiative such as the NIH sIRB policy and revised Common Rule make it clear that ...

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Blog

Checklist to Reduce Burden on Sites and Patients

Review a list of considerations for site-sponsor tasks to streamline startup, reduce redundancy, and refine technology choices for effective partnerships.

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5 min. read
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Blog

Enhancing User Experience, Security, and Compliance with Single Sign-on

As technology evolves and the industry streamlines research workflows, implementing SSO can lead to significant improvements in both user experience and security.

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5 min. read
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Webinar

Navigating sIRB Complexities: An Interactive Session

Upcoming: March 26

Join us as we share insights, strategic priorities, and guidance for preparing your institution for sIRB mandates.

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Webinar

Sponsors: Are Your Sites Ready for an FDA Inspection?

Learn a comprehensive overview to prepare sponsors and sites for an FDA inspection.

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Webinar

Re-Air: Faster Trials, Successful Sites, Empowered Patients: Improve Your Research Experience

Upcoming: March 21

Optimize clinical trials with practical solutions, real site feedback, and tools for seamless success. Join our webinar to revolutionize your research approach.

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E-Book

How to Improve Your Site Compliance

Many clinical trial sites face challenges to stay compliant on a study. It is important for sites to adhere to the myriad of requirements that constitute Good Clinical Practices (GCP).

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Blog

IRB Review of Changes to Previously Approved Research

Make sure you know the IRB review requirements for amendments involving changes to IRB-approved protocols and other study modifications.

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5 min. read
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Blog

Optimizing Site Initiation Timelines Through Centralized Processes

Learn how to optimize clinical trial initiation with centralized processes, intuitive intake forms, and custom reporting and streamline workflows for efficiency.

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3 min. read
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Blog

mRNA Cancer Vaccines and Therapies: An Overview

Learn about mRNA’s potential impact on cancer research, the technology’s unique challenges, and strategies for researchers developing mRNA-based cancer studies.

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4 min. read
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