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Blog

Beginner’s Guide to Medicare Coverage Analysis

Medicare coverage analysis evaluates how clinical research protocol items and services are billed per federal agency guidelines.

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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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Blog

Developing and Implementing a Successful eConsent Process

As the industry continues to shift from brick-and-mortar trials to more convenient hybrid formats, eConsent proves to be useful.

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4 min. read
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Blog

Privacy Regulations Impact on Global Clinical Trial Endpoint Adjudication

Endpoint adjudication committees must keep up with rapidly developing requirements as they receive potentially identifiable research data.

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5 min. read
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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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3 min. read
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Case Study

Investigating Enrollment Reliability with the Longboat Platform

Download the case study to learn if the Longboat Platform helps sites more accurately set and reach their patient recruitment targets.

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Webinar

How to Optimize Your sIRB Experience

Upcoming: February 2

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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3 min. read
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Case Study

Ensuring Recruitment and Compliance Success of an Evolving Rare Neuromuscular Disease Study

Find out how the Longboat Platform ensured not only recruitment success, but site and participant support and compliance.

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Webinar

Rare and Orphan Diseases in Regulated Development

In this webinar, gain an in-depth understanding of regulatory and clinical development challenges for rare/orphan diseases.

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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

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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5 min. read
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