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No Code EDC Platform:
A New Era in Clinical Trial Efficiency and Flexibility

Jean-Pascal Rugiero

28 Jan 2025

In the ever-evolving landscape of clinical trials, efficiency, accuracy, and speed are paramount. Electronic Data Capture (EDC) platforms have revolutionized data management by transitioning from paper-based systems to digital solutions. However, the complexity of traditional EDC platforms often introduces delays and errors. No Code EDC systems, such as DISTILL, have a transformative approach that simplifies trial setup and data capture without requiring any coding expertise. This white paper explores how No Code EDC platforms streamline clinical trials, saving time, reducing errors, and ultimately accelerating study timelines.

 

What is No Code EDC?


No Code EDC platforms empower users to design and manage clinical trials with no programming knowledge. These platforms offer intuitive, user-friendly interfaces that allow researchers and clinical operations teams to configure data entry forms, validation rules, logic and study workflows through drag-and-drop functionalities, tick boxes and pre-built templates. The result is a more accessible and flexible tool that aligns with the fast-paced demands of clinical trials.

 

Simplifying Trial Setup and Data Capture


  1. Streamlined Configuration: Traditional EDC systems often require intricate coding for study setup, which can be both time-consuming and error prone. No Code EDC platforms eliminate this barrier by providing visual design tools that allow users to set up study protocols, data forms, and validation rules through a graphical interface. Researchers can create and modify data entry forms with ease, ensuring that the system reflects the study's requirements accurately.


  2. Reduced Training Time: With No Code EDC, the learning curve is significantly reduced. Users do not need to acquire programming skills or rely on specialized IT support to configure the system. Instead, they can focus on their core tasks, such as designing study protocols and monitoring data quality, leading to faster implementation and smoother trial execution.


  3. Enhanced Flexibility: No Code EDC platforms offer built-in flexibility to adapt to changing study requirements. As trial protocols evolve, users can quickly adjust data entry forms, validation rules, and workflows without the need for complex programming changes. This adaptability ensures that the EDC system remains aligned with the study's objectives throughout its lifecycle. Modifications can be done easily, with no down time and at no cost.


  4. Minimized Errors: By simplifying the configuration process and offering pre-built templates and validation rules, No Code EDC platforms reduce the likelihood of errors in study setup. The visual interface and built-in checks help prevent common mistakes and ensure that data is captured accurately and consistently.

 

Case Studies: Accelerating Study Timelines

 

Case Study 1: Reducing Study Setup Time

 

A mid-size CRO was managing a large Phase III clinical trial involving multiple sites and complex protocols. Previously, setting up the EDC system for such a trial required extensive coding and IT support, resulting in a setup time of 8 to 10 weeks with a classic EDC.


By using a No Code EDC, the CRO was able to reduce the setup time to just 2 weeks, including eCRF build, UAT and full study setup. The intuitive design tools allowed the study team to quickly configure data entry forms, validation rules, and study workflows without relying on IT departments. This reduction in setup time translated to a faster start for the trial, accelerating the overall study timeline and enabling quicker data collection and analysis.


This CRO later went on working on their second study with it and they were able to go even faster, being used to how easy setup was.

 

Case Study 2: Enhancing Data Accuracy in a Multi-Site Study

 

In a multi-site clinical study, a pharmaceutical company faced challenges with data accuracy and consistency due to variations in data entry practices across sites. Traditional EDC systems with complex coding requirements made it difficult to enforce uniform data entry standards.


By adopting a No Code EDC platform, the company was able to standardize data entry forms and validation rules across all study sites. The platform's built-in templates and visual design tools enabled the study team to implement consistent data capture protocols effortlessly. As a result, data accuracy improved significantly, and the study's overall data quality was enhanced, leading to more reliable and actionable results.

 

Case Study 3: Accelerating Data Cleaning and Monitoring

 

A biotech company running a global clinical trial needed to streamline data cleaning and monitoring processes. Traditional EDC systems required manual intervention and extensive coding to set up data validation rules and monitoring reports, causing delays in identifying and resolving data discrepancies.


With a No Code EDC, the company was able to automate data validation and monitoring through easy-to-configure rules and reports. The platform's real-time data monitoring capabilities and dashboards enabled faster detection of issues and more efficient data cleaning processes.

 

Conclusion

 

No Code EDC platforms represent a significant advancement in clinical trial management, offering a streamlined, efficient, and user-friendly approach to data capture and study setup. By eliminating the need for IT coding, these platforms simplify trial design, reduce errors, and accelerate study timelines. The case studies presented demonstrate the tangible benefits of adopting No Code EDC solutions, highlighting their potential to transform clinical trial operations and enhance overall study efficiency.

  

Typical implementation of a classic EDC system takes 16-20 weeks.


No code EDC implementation will take 4-8 weeks, 1-2 weeks with DISTILL.

As clinical trials continue to evolve, No Code EDC platforms stand out as a powerful tool for optimizing data management and achieving faster, more accurate results. For organizations looking to stay ahead in the competitive field of clinical research, embracing No Code EDC technology may well be the key to unlocking new levels of efficiency and success.


For further information on No Code EDC platforms in general and on DISTILL in particular, please contact at jay@distill.biz.

Distill Technologies LLC


3701, Churchill Executive Tower
Business Bay, Dubai, UAE

enquiry@svmpharma.com

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