Transforming data into differentiation throughout the clinical journey.

Kickstart your molecule’s journey with Strong Tower’s scalable and validated statistical computing environments. From biomolecular analysis to early safety assessments, our platforms, including validated and unvalidated SAS and R environments, are designed to streamline data ingestion processing and analysis. Overcome the mounting challenges of intense data volumes and complex analyses with cloud-based data science platforms that ensure your early-stage research is compliant while anticipating the requirements of your next step in the journey.

As your molecule advances through the pivotal clinical stages, reliability and agility in data management are paramount to success. Strong Tower’s expertise in SAS Integration and R & Python interoperability allow for seamless cross-platform communication and support the dynamic needs of your program as it moves through the clinical trial. Our Posit Connect solution facilitates the creation of a transparent and reproducible analysis workflow for biostatistics. Meticulous attention to detail during environment set up and version control together streamline regulatory compliance to keep your trials on track.

After the commercial launch of your molecule, the focus shifts to real-world evidence gathering, market analysis, and ongoing safety monitoring. Our cloud-based platforms transform the delivery of analysis-ready data from months to days, enabling rapid response to market dynamics and regulatory inquiries. Leverage our proven track record in delivering high-powered data management and reporting solutions to gain insights that drive commercial success and inform lifecycle management strategies.