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Blog

Why Now is the Right Time to Adopt eConsent

A valuable tool for both sites and participants, now is the right time for sites to adopt an eConsent platform.

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Webinar

How to Optimize Your sIRB Experience

Find out how other institutions have used sIRB requirements as an opportunity to elevate their research programs in this webinar.

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Blog

Beginner’s Guide to Budget Negotiation

Proper trial financing ensures internal costs are covered, facilitates better negotiation, and leads to higher compliance in trials.

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Blog

Beginner’s Guide to Single IRB Mandates

More governing bodies are starting to opt for single institutional review board (sIRB) review as a way to streamline research operations.

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5 min. read
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Blog

Medicare Coverage Analysis Worksheet

Determine whether your trial meets the requirements of the National Coverage Determination (NCD) for Routine Costs in Clinical Trials.

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5 min. read
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Blog

Your Guide to sIRB Mandates

sIRB regulations and policies have been announced and implemented to help address the challenges of conducting clinical trials involving multiple research sites.

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4 min. read
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Blog

Why Keep HIPAA Separate from the Informed Consent Form

HIPAA is important to the informed consent process, and oftentimes, a standalone document is the most beneficial approach.

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Blog

Regulatory Trends in Cell and Gene Therapies

Recent signals have indicated the FDA plans to provide greater support for cell and gene therapy research.

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6 min. read
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Blog

Understanding FDA’s Draft Guidance on Ethical Considerations for Involving Children in Clinical Trials

Until the 1980s, children were excluded from research studies. Now, FDA provides draft guidance on ethically including kids in trials.

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Blog

FDA’s September 2022 NPRMs: What They Mean for Academia and Industry

FDA’s new NPRMs would harmonize certain IRB regulations with the HHS Common Rule. Find out what this could mean for sites and sponsors.

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E-Book

Setting Yourself up for Success During Investigator-initiated Trials

This eBook shares tips and best practices to guide researchers through the investigator-initiated trial process while staying compliant.

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Webinar

Addressing Decentralized Pre-Enrollment Challenges for Sites and Site Networks

Learn key processes and tools for your team to use to ensure your organization operates at peak performance.

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