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The development and implementation of clinical interventions is a complex, iterative and time-consuming process that takes years before discoveries in biomedical research result in health benefits for patients and communities.

Read about Dr. Matthew Cherian's research

The Medical Modeling, Materials and Manufacturing (M4) Division of the Center for Design and Manufacturing Excellence (CDME) is where medicine, manufacturing and materials-related development converge to create healthcare solutions.

Recruitment and Retention granted the award

The CCTS Recruitment and Retention program helps inform researchers of the various strategies and best practices to recruit participants. The program helps increase the likelihood that potential participants will learn about and participate in clinical trials.

By CCTS Director and PI, Dr. Julie Johnson, PharmD

The Ohio State University Libraries provides open access initiatives by covering fees for eligible articles through various publishing agreements.

ConsentTools helps clinical research professionals understand and adopt three evidence-informed practices for informed consent in clinical trials. These practices assess and improve participant understanding of clinical trial information, and assist professionals in appointing legally authorized representatives (LARs) when necessary.

The course features weekly facilitated discussions from experts across campus.