Given the ongoing complexity in the healthcare marketplace and the need for constant business performance improvement to reduce costs and increase revenue, new, real time, dynamic tools, and metrics help make decision making easier for those who work in the healthcare industry. We’ll be presenting success stories and thoughtful insights on the ongoing changes in the industry,  how the better use of data can improve patient care, drive performance improvement, and increase revenue.

Choosing the right bioanalytical platform for your immunology or vaccines clinical trial is critical to data collection. But navigating the intricate bioanalytical process and selection of assay platforms can be difficult. What do these platforms look like in use, and how should you go about selecting the right one? This webinar will demystify the bioanalytical requirements for clinical studies and will discuss the most common bioanalytical platforms used during clinical trials to measure vaccine responses and levels of inflammatory mediators in biological fluids.

Choosing the right bioanalytical platform for your immunology or vaccines clinical trial is critical to data collection. But navigating the intricate bioanalytical process and selection of assay platforms can be difficult. What do these platforms look like in use, and how should you go about selecting the right one? This webinar will demystify the bioanalytical requirements for clinical studies and will discuss the most common bioanalytical platforms used during clinical trials to measure vaccine responses and levels of inflammatory mediators in biological fluids.

Biosecurity risks are a wide and diverse field that isn’t limited to what’s in your labs. There are many different types of players across the globe. Join our two experts to learn much more.

Panelists: Yong-Bee Lim, PhD, Fellow, Council of Strategic Risks
> Kathleen Vogel, PhD, Director + Professor, School for the Future of Innovation in Society, ASU

In this webinar, we’d like to introduce Avéma Pharma Solutions, a contract manufacturer with the capabilities that pharma companies need when selecting a CDMO including in-house R&D capabilities, formulation development, full analytical labs, process scale up and transfer expertise, development and validation of analytical methods, pilot scale and commercial manufacturing capabilities, and regulatory support. As an organization focused on speed to market, we can help you launch your products quickly, efficiently and cost effectively.

This event will feature a mix of industry leaders and pioneers sharing first-hand lessons learned from their pioneering case studies accelerating the development of medical device software at the dawn of the age of digital health. During this webinar, they will share best practices and worst practices learned through their leading edge efforts. They will discuss a variety of tech industry approaches to leverage such as fast feedback loops (e.g., agile and Lean Startup), design thinking, and non-traditional leadership approaches, and how to best fuse those approaches with the constraints and decades of experience already known in regulated MedTech.