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The iMednet eClinical platform offers a cost-effective solution with a full suite of native tools to simplify and shorten study build times, increase efficiency in study execution, and minimize costs through the duration of the study.

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FDA COVID-19 Guidance for Clinical Trials

FDA COVID-19 Guidance for Clinical Trials

The COVID-19 pandemic continues to impact our lives in many ways, and the clinical research industry is no exception. Clinical research and the potential for improving health and delivering life saving treatments must continue, not only to address and mitigate the...
Transforming Clinical Studies During Pandemic

Transforming Clinical Studies During Pandemic

In the past several weeks, much has changed for all of us. The COVID-19 pandemic and social distancing guidelines are adding new pressures across all aspects of our lives, and we know clinical trials are no exception. During these challenging times, our team at Mednet...
Review of FDA Guidance for Adaptive Trial Designs

Review of FDA Guidance for Adaptive Trial Designs

This is the third installment of a three-part blog series on Complex Innovative Trial Designs.  As we’ve discussed previously, clinical trials are evolving rapidly, with new data sources and medical innovation increasing the complexity of study designs. The FDA...
FDA’s Guidance on Complex Innovative Trial Designs

FDA’s Guidance on Complex Innovative Trial Designs

As discussed in our last blog, with advances in medical science and new data sources, study design complexity is on the rise. The US FDA continues to show interest and support for these new and innovative science and clinical trial designs, initiating programs and...