Don’t let the ever-changing regulatory environment fracture quality management systems you have in place for clinical trials. Meet and beat those challenges. Our newest webinar helps you move through the Innovation Curve – allowing you to dig out of the Trough of Disillusionment to speed up the Slope of Enlightenment. The end goal? You see clearly how technology really can eliminate the complexity too often found in today’s rapidly evolving digital world.
Join endpoint’s, VP Data and Quality, Cat Hall as she talks about facing and overcoming quality management system challenges, industry regulatory trends, and understanding today’s digital trial systems environment.
Cat Hall, VP Data and Quality, endpoint
Cat Hall started her career as an academic scientist in molecular and cellular biology before finishing her MBA and transitioning into pharmaceutical supply chain management. During her career, she developed notable expertise not only in clinical supplies but also in training development, process improvement, managing partnerships and the design and implementation of technologies such as IRT. She is well-known for focusing on bridging the GMP/GCP gap by bringing supply chain customer service through the last mile to patients. Cat joined endpoint in 2019 as VP of Product Strategy to help continue to bring the customer voice forward into shaping the future of IRT.Message Presenter
Who Should Attend?
Senior professionals working in in Clinical Trial Management, including those involved in:
- Data Quality
- Quality Systems
What You Will Learn
- Thorough understanding of today’s digital clinical trial systems
- Significant trends in audits and regulatory inspections
- Common challenges to digital quality management systems
- How to manage and overcome those challenges once and for all
endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE® platform, have proven to maximize the supply chain, minimize operational costs, and ensure timely and accurate patient dosing. endpoint is headquartered in San Francisco, California, with a global footprint in the APAC region and Europe.