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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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eClinical Resources

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Understanding the Site User Experience: Results from the 2022 iMednet End User Survey

Resource Type: Blog
Solutions: Customer Success, Electronic Data Capture (EDC), Study Startup

Earlier this year, the Mednet team wrapped up our annual 2022 End User Survey. While it is important the iMednet platform is flexible and easy to use for our sponsor and CRO customers, it’s critical the platform is also easy to use across clinical trial sites.

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Evolving Requirements for Trial Supply Management

Resource Type: Blog
Solutions: Decentralized Clinical Trials (DCT), Electronic Data Capture (EDC), Randomization & Trial Supply Management (RTSM)

Numerous factors are changing the way clinical trials are conducted. Increasingly complex trial designs, global patient groups, and decentralized trial models have significantly impacted how trial information is tracked and managed. These factors have also influenced how clinical professionals manage trial supply and inventory.  

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Driving Innovation in Clinical Trials at SCOPE Summit 2022

Resource Type: Blog
Solutions: Clinical Trial Trends

As always there are an abundance of topics being discussed and presented by clinical research thought leaders around the world – with the theme, Driving Innovation in Clinical Trials and Digital Health.

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Looking Ahead to Clinical Trial Trends in 2022

Resource Type: Blog
Solutions: Clinical Trial Trends, Decentralized Clinical Trials (DCT)

In the past two years, we have seen quick and substantial pivots in the way clinical trials are conducted. Every aspect of a trial has been reshaped, repackaged, or completely transformed.

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Why Adaptive Trial Designs Require Adaptable Technology

Resource Type: Blog
Solutions: Biotechnology, CROs, Medical Device, Pharmaceutical

Adaptive trial designs emerged as a means to improve clinical trials based on all available information. High failure rates and increasing costs have driven the industry toward adaptive trial designs….

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What Does Real World Data Mean to Clinical Trial Teams?

Resource Type: Blog
Solutions: Biotechnology, CROs, Medical Device, Pharmaceutical

Introduction  Real-Word Data (RWD) and Real-World Evidence (RWE) are acronyms that have been thrown around the industry for some time. As healthcare, life sciences companies and regulators look at the potential research opportunities that stem…

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Breast Cancer Research: Where Complexity Demands Flexibility

Resource Type: Blog
Solutions: Biotechnology, CROs, Medical Device, Pharmaceutical

October is Breast Cancer Awareness Month. The National Breast Cancer Foundation estimates one in eight women in the United States will be diagnosed with breast cancer in her lifetime.1 Most of us know a friend or family…

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SCDM Live Global Conference 2021 Key Takeaways

Resource Type: Blog
Solutions: Biotechnology, CROs, Medical Device, Pharmaceutical

For those who attended the SCDM Live Global Conference, the futuristic style of the virtual meeting and the theme (Future Now: v.2.021) did not disappoint. The conference last week broke…

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Looking Ahead to the SCDM 2021 Program

Resource Type: Blog

Mednet is excited to once again be a sponsor of the Society of Clinical Data Management’s (SCDM) Global Conference, September 26 – 29. The conference is virtual this year, and the theme is “Future Now v2.021”, which is particularly fitting considering the…

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Reducing or Eliminating Traditional Barriers in Clinical Trials

Resource Type: Blog
Solutions: Biotechnology, CROs, Medical Device, Pharmaceutical

Prior to the pandemic, there was a growing interest in shifting clinical trials to virtual or decentralized models to boost patient recruitment, improve retention, reduce costs and more. The pandemic only accelerated…

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