Navigate clinical trials with confidence.

Strong Tower employs a multi-faceted approach to protect the accuracy and integrity of your sensitive clinical trial data. Firstly, we implement robust version control mechanisms, which track changes to data sets and ensure that the most up-to-date and accurate information is used for analysis. This helps prevent errors and discrepancies that may arise from using outdated or incorrect data. Additionally, we ensure seamless integration across platforms, allowing for smooth data transfer and analysis between different systems and tools. By minimizing data transfer errors and ensuring consistency across platforms, Strong Tower helps to maintain the reliability of your most valuable asset, your clinical trial data, to support enhanced decision-making and regulatory compliance.

Strong Tower recognizes the dynamic nature of clinical trials and the need for adaptability in response to changing trial conditions and regulatory requirements. Our platforms are designed to enable swift adjustments to evolving trial protocols, patient populations, and regulatory standards. For example, our Posit Connect solution facilitates transparent and reproducible analysis workflows, allowing researchers to quickly adapt to new data demands and regulatory requirements without compromising data integrity. Additionally, our team works closely with clients to anticipate potential challenges and proactively implement solutions to address them. By fostering adaptability and flexibility in clinical trial operations, Strong Tower helps clients stay agile and responsive in the face of the many changes that occur over the course of a clinical program.

Laser focused on serving the highly regulated pharmaceutical space, Strong Tower is adept at maintaining compliance with all applicable regulatory standards throughout the clinical trial journey. We pay meticulous attention to detail in all aspects of data management, ensuring that data collection, processing, and analysis adhere to both regulatory requirements and industry best practices. Additionally, we provide robust statistical analysis tools like JMP Clinical, which are specifically designed to support compliance with regulatory standards such as those set by the FDA. These tools help researchers generate accurate and reliable results that meet regulatory scrutiny. Furthermore, our team stays abreast of changes in regulatory requirements and works closely with clients to ensure that their clinical trial processes remain compliant as regulatory scrutiny increases throughout the clinical trial process and beyond. By prioritizing compliance at every stage of the clinical journey, Strong Tower helps clients navigate regulatory challenges with confidence and integrity.