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EVERSANA Announces Real-World Data Agreement with Janssen
Analytic work will drive regulatory grade RWD studies and therapeutic evidence to improve patient outcomes.
EVERSANA today announced an agreement with Janssen Research & Development, LLC (Janssen) to transform clinical data into the much-needed evolution of chronic disease care through real-word data (RWD), data science analysis and regulatory-grade studies. The collaboration between EVERSANA’s RWD Solution team and the Janssen Research & Development Data Science team will help drive evidence-based development of Janssen therapies, treatments, and patient support models.
The agreement will drive a deeper understanding and enhance the design of clinical trials through regulatory-grade, auditable determination of clinical endpoints, thus enabling studies that can reduce clinical trial timelines and offer important signals about how therapies perform in real world settings.
Read more about the new agreement here.
What Every Pharma CEO Should Know About Unlocking the Potential of Scientific Data
December 11th 2024When integrated into pharmaceutical enterprises, scientific data has the potential to drive organizational growth and innovation. Mikael Hagstroem, CEO at leading laboratory informatics provider LabVantage Solutions, discusses how technology partners add significant value to pharmaceutical R&D, in addition to manufacturing quality.
Key Findings of the NIAGARA and HIMALAYA Trials
November 8th 2024In this episode of the Pharmaceutical Executive podcast, Shubh Goel, head of immuno-oncology, gastrointestinal tumors, US oncology business unit, AstraZeneca, discusses the findings of the NIAGARA trial in bladder cancer and the significance of the five-year overall survival data from the HIMALAYA trial, particularly the long-term efficacy of the STRIDE regimen for unresectable liver cancer.
