These days, top-tier biopharma companies are using real-world data (RWD) to power their cardiovascular disease research. With so many sources of data, both in-house and licensed, we know it can be hard to sort through it all and analyze what you need to answer your research questions. Download now.

While the global demand for medical devices is rising, the industry is facing revenue and supply chain pressures. To address these, medtech manufacturers must reduce costs, and conducting clinical trials more efficiently is a key piece of that puzzle. In this paper, we explore best practices medtech can adopt from biopharmaceutical clinical trials. Download now.

Want to know how healthcare providers (HCPs) would like to interact with your brand regarding market access? To find out, we surveyed 100 actively practicing physicians on a range of topics that impact market access pull-through. Download now.

Characterizing Degrader molecules generally requires the determination of DC₅₀ values using traditional western blot. But the lengthy, manual workflow and resulting low reproducibility make it an unreliable approach. Simple Western provides reproducible DC₅₀ values in about 3 hours. Read how.

Modern software development approaches are key to the life science industry’s ability to better manage clinical trial complexity, derive value from massive volumes of data, and surmount fragmented technology solutions. Download now.

Join us at the Fierce Clinical Summit as we share best practices for ensuring clinical trial integrity and inspection readiness through effective oversight of internal, vendor and site operations. This is THE annual in-person gathering for clinical quality professionals!