Services / Data Management / Legacy Code Automation

Automate tasks to streamline clinical trial workflows.

Managing manual processes and code writing in clinical trials is a significant obstacle that can hinder efficiency, accuracy, and regulatory compliance.

Automation in clinical trials addresses the challenges of manual quality checks, data processing, and integration of older systems with modern technologies, processes that are often cumbersome and error-prone, demanding significant time and resources. Strong Tower offers legacy code automation services that enhance efficiency, security, and accountability, allowing clinical trial organizations to focus on what matters most—advancing medical research and development.

Today’s clinical trial data requires a new standard of efficiency.

Automate Quality Checks

Our legacy code automation enables the execution of streamlined quality checks, which are traditionally manual and error-prone. By setting up these checks automatically within our easy-to-use interface, you can ensure that your data meets the highest standards of quality and accuracy, without the need for manual intervention or newly written code.

Enhance Data Security

Strong Tower’s legacy code services include robust security features that track every step of the process, ensuring that your data remains secure and compliant with regulatory standards. Our automated systems identify and address potential vulnerabilities in legacy code, protecting sensitive trial data.

Integrate with Existing Workflows

We understand the importance of leveraging your existing investments in SAS macros into the CAAS pipeline, eliminating the need for multiple programs to manage your data sets. Our legacy code automation service seamlessly integrates into your workflows in a centralized platform that provides functions such as edit checks, safety dashboards, and auto-sequencing. This integration streamlines processes, enhances your current pipeline, and ensures continuity and consistency across all phases of your clinical trials.

Improve Data Organization

By automating the conversion of data and metadata sets into SAS datasets, we eliminate tedious management tasks and the risk of human error. Our solution keeps track of your files by managing labels, formats, and dates, ensuring that your data is always up-to-date and ready for analysis. This automation not only saves time but also reduces errors, leading to more reliable trial outcomes.