Resource Library

Your RTSM sits at the intersection of your master protocol and data management processes. Being prepared to answer vendor questions on these topics can speed up study build timelines and ensure that your RTSM technology is optimized to support your success.

Join Freenome's Yontao Lu, Ph.D., and Aijing Gao, along with Medrio's Melissa Newara, as they discuss best practices and share case studies on how to achieve scale without compromising patient needs.

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.

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.