Medrio Blog

Importance of Quality Data in Meeting Increasing FDA Regulatory Scrutiny

Partnering with a reliable EDC vendor to ensure your clinical trial data meets high standards of accuracy and integrity is essential for passing FDA scrutiny. Risk-based approaches and improved monitoring workflows can help researchers stay ahead of the curve in navigating any potential challenges posed by the FDA, reducing the risk of warnings, rejections or costly additional research.

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Maximizing Data Efficiency: Practical Database Design Tips

Effective database design is essential for successful clinical studies, as it improves data quality and accuracy and increases the speed of trial times. This can be done by ensuring the database is user-friendly, utilizing new technologies such as eSource, regularly checking data trends, focusing on SDTM while designing the database, and consulting with sites to proactively address any irregularities. Ultimately, accelerated trial times rely heavily on effective database design.

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How to Differentiate Your CRO in Today’s Market

To stand out in a competitive CRO market, CROs must differentiate themselves by utilizing innovative clinical trial technology and trusted partners like Medrio. This collaboration can lead to efficient builds, reduced timelines, and seamless client experiences, ultimately setting the CRO apart.

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5 Ways To Prevent Costly Database Delays

Delays in a clinical trial process can have serious downstream consequences, such as missing a go-to-market window or preventing life-changing solutions from reaching the people who need them as soon as possible. Here are five tips to reduce the risk of database delays.

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