Join us for this webinar and learn how Medidata eTMF manages all your data and content - from study planning to close - on one platform, accelerating study startup and ensuring compliance & inspection readiness. Register now!
A rising global demand for more minimally invasive surgeries to treat both cardiovascular and peripheral arterial diseases are driving the market to look for new and more efficient materials to construct stent grafts used in those procedures. Download this whitepaper to learn more about DSM and the benefits of using the Dyneema Purity® membrane.
Risk assessment is a very important first step in an organization’s overall monitoring efforts and a major driver for sponsors’ monitoring efforts - as detailed in the amended ICH E6 GCP (good clinical practice) guidelines on risk assessment. This webinar will focus on understanding ICH E6 as the main driver of an end-to-end risk management approach. Register Now.
With cloud computing capacity growing all the time and machine learning tools coming online, marketeers’ ability to quickly and easily ask questions of the data will also increase. Learn more. Download it now!
Join Qlik and Dark Matter to learn how Life Science and Healthcare companies use visual big data analytics to quickly explore billions of medical claims, physician and patient data to accelerate patient recruitment and meet patient accrual goals. Register now.
The Pharmacokinetics (PK) of ADC therapeutics typically show a discrepancy between the PK of total antibody and that of conjugated antibody, carrying one or more payload molecules. This will present how quantitative systems pharmacology modeling approaches provide biological insights into the impact of drug-to-antibody ratio and the resulting changes in molecular properties on overall PK and relative payload disposition as observed in preclinical and clinical studies. Register now!
The life sciences industry is undergoing a digital transformation, as legacy IT systems move into the cloud and cohesive transition strategies are required. Whether you’re in Quality Control, Clinical Operations, IT, Regulatory Compliance, or manage another area of the trial, join Medidata and Box explore how to build a total regulated and non-regulated content management strategy to match today's unique challenges, including implementing technology via a single, user-friendly platform. Register now!
While biopharmaceutical companies face challenges in generating and integrating meaningful insights that drive timely and actionable decisions. Aggregating and leveraging the right data to drive value requires a broad range of services working together to generate insights across the entire drug development spectrum. Hear PAREXEL experts derive data-driven insights and how these insights can benefit many essential drug development areas. Register now!
Quality. Speed. Simplicity. Learn how a new elastomeric closure formulation, turnkey extractables and leachables package and a flexible supply can help generics manufacturers make the move to market. Join this webinar with West experts and learn about generics market trends and AccelTRA™ brand program attributes that address generic injectable drug manufacturer issues and ensure a fast move to market. Register now!