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.
Attend this webinar to hear from experts on how to overcome challenges when developing a robust upstream cell culture process and scaling to large scale manufacturing. Register Now.
In the quest to understand how a therapeutic intervention performs in actual use – in real medical practice outside the controlled environment of clinical trials – many life sciences organizations are stymied. They rely on one-off processes, disconnected tools, costly and redundant data stores, and ad hoc discovery methods. Download now to read more.
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!
This executive summary will explore how to drive excellence within the forecasting process and how to utilize forecasting throughout the clinical study to better plan clinical supply budgets and project timelines and to identify potential supply-related issues before they negatively impact your study. Download it 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!
Join this webinar to learn how real world data is transforming the way biopharma, CROs and study sites navigate obstacles in drug development, the impact of real world data on clinical trials, and the appropriate use cases to incorporate real world data in the planning and execution of clinical trials. Register now!
The use of the cloud for regulated workloads can transform how companies think about their compliance practices. Cloud-based regulated workloads can improve auditability, transparency, and consistency, as well as offer scalability, transparent costs, and a reduced need for on-premises hardware systems. Download this whitepaper to learn about GxP in the AWS cloud and the compliance and efficiency benefits of rethinking regulated workloads. Download this Whitepaper now!