Patient Enrollment and Retention in Clinical Trials

Patient accrual and retention strategies – increasing enrollment and improving study visits and patient engagement in clinical trials.

5 Takeaways for More Patient-Centric Clinical Trials

June 21st, 2017 by Mel Johnson

Expert panelists address key challenges and opportunities for increased patient centricity in clinical trials.

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How to Engage Healthcare Providers and Encourage More Clinical Trial Referrals

February 2nd, 2017 by April Schultz

Increase the number of motivated patients recruited to your clinical trial through strong relationships with physicians and nurses.

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Predicting Enrollment: 6 Tips for Sites to Estimate the Right Number

January 12th, 2017 by Kristina Lopienski

Navigate the difficulties of predicting clinical trial enrollment numbers with these six tips for more accurate enrollment estimates.

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Holiday Tips for Avoiding Stress and Staying Focused on Your Research

December 1st, 2016 by Ryan Monte

To keep staff and trial participants happy during the holiday season, research sites need to be proactive.

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Top 4 Barriers to Patient Participation in Clinical Trials

November 22nd, 2016 by Anna Hrovat-Staedter

Identify solutions to common barriers that inhibit patient participation in clinical trials.

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Automating Your Participant Payments Empowers Your Staff and Subjects

October 25th, 2016 by Ryan Monte

Automating your participant payments can do more than just streamline your workflows. Learn how it can impact your subjects, staff and organization as a whole.

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Rethinking Engagement for More Repeat Trial Participants

September 22nd, 2016 by April Schultz

Encouraging repeat trial participation through extended participant engagement and open communication.

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5 Questions to Enhance Your Clinical Trial Enrollment Planning

July 12th, 2016 by April Schultz

Answer these questions to create a solid subject enrollment plan and increase the success of your patient recruitment campaigns.

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Making Your Consent Forms Readable: The Why and the How - Q&A

June 29th, 2016 by Dr. Wendy Tate

In this Q&A, Dr. Wendy Tate of Nimblify, Inc. answers attendee questions from her webinar "Making Your Consent Forms Readable: The Why and the How." Question topics include NPRM, federal regulations, cost language, central IRBs and more.

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Websites for Clinical Research Sites: Where do I Start?

June 23rd, 2016 by Kayla Leverton

Squarespace is one of several easy-to-use website design platforms available to clinical research sites looking to redesign their website.

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