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eConsent is transforming the informed consent process, making it easier for would-be trial participants to understand what's required of them and providing sponsors with real data on participant comprehension. It's an important step towards a future of secure, efficient clinical research that serves everyone involved.

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.

Digital tools like ePRO and eConsent have transformed clinical trials, allowing for faster and more efficient experiences with improved data accuracy. However, choosing the right partners and products that generate high-quality data and frictionless workflows is crucial for clinical studies.

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.

Medrio EDC has boosted HMR's Statistics & Data Management group with an intuitive build functionality, automated query firing, and skip logic, increasing efficiency and accuracy. This scalable solution offers cost-effective data quality and exceptional service levels for sponsors, making the transition from paper-based processes seamless.

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.