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To Pay or Not to Pay: The Ethics of Participant Payments

Should participants be paid for clinical trials or not? A look at ethics literature.

Q&A Part II: How Protocol Feasibility Assists in Promoting Compliance

In this Q&A, Dr. Wendy Tate answers attendee questions from her webinar “How Protocol Feasibility Assists in Promoting Compliance.”

Forte’s Top 10 Clinical Research Resources of 2019

We strive to create meaningful and relevant content for the clinical research industry. Check out our top 10 resources of 2019.

Q&A Part I: How Protocol Feasibility Assists in Promoting Compliance

In this Q&A, Dr. Wendy Tate answers attendee questions from her webinar “How Protocol Feasibility Assists in Promoting Compliance.”

PRIM&R AER Conference: Collaborating to Advance Ethical Research

The 2019 PRIM&R AER Conference provided insights into the changing regulatory world, and reaffirmed the importance of technology as processes and regulations continue to evolve.

3 Tips to Keep in Mind When Preparing for Your Next Audit

At any research site, audits are inevitable. Check out these tips and tricks to help prepare your site for your next audit.

Diving Deeper into Clinical Research: Recommended Reading for Research Staff

Knowing and understanding the history of clinical research is just as important as knowing present-day roadblocks and best practices. Check out our recommended reading list.

Tips for Successful Clinical Trial Budget Negotiations

Effective budget negotiation is consistently a hot topic for clinical research sites. Here are a few tips to make sure your site gets the most from your negotiations.

Social Media Marketing for Patient Recruitment

With recruitment challenges on the rise for sites, consider finding potential participants on social media.

Top 6 Challenges in Informed Consent

Informed consent is important to any clinical trial – but that doesn’t mean it comes without challenges. Read more about the top 6 challenges research institutions face.

The Beginner’s Guide to Implementing an Enterprise eRegulatory Management System

Many sites understand the benefits of moving from paper regulatory binders to an electronic system. But it’s also important to ensure your organization is implementing a system that will fit your regulatory workflows and set you up for long-term success.

Performing Protocol Feasibility Assessments to Enhance Clinical Trials

Protocol Feasibilities are designed to help clinical research staff determine the possibility of conducting a study. Here’s how to seamlessly work an assessment in before accepting your next clinical trial.

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