The Importance of Data Integrity and Accessibility in Successful Clinical Trial Management
About this webinar
A Chat with Industry Experts in Quality and Data Management about how Data is Reshaping the Industry
In today’s digital world, data is king, and the future is in robust systems and processes that ensure data integrity and value. Within the clinical trial industry, data is collected in many formats, and it must be filtered and managed to be useful. Controlling how it is stored, accessed and ultimately used is all part of assuring data reliability and protecting the safety of patients and the quality of the drugs created.
In this webinar, the featured speakers will talk all things data — how it’s relevance and accessibility has flourished, how it’s shaping the clinical trial industry and the expected growth of data strategy as technologies and the roles in data management evolve.
Register for a chat with industry experts in quality and data management about data integrity and accessibility for successful clinical trial management. We invite you to submit your topics and questions in advance for the discussion.
Who should attend
- Quality and Audit Management and Support
- Data Management
- Data Scientists and Analysts
- Clinical Trial Planning and Optimization
- Clinical Operations Management
What you will learn
- The 5 V’s of data
- Evidence of the need for automation in data driven activities
- How roles are changing to support today’s clinical trial data
- Steps to implement a successful data management strategy
Featured Speakers
Cat Hall
Cat Hall started her career as an Academic Scientist in molecular and cellular 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.
Patrick Nadolny
Patrick Nadolny has almost 30 years of industry experience across pharmaceutical, device and biologics as well as technology solution development. He is a pragmatic leader focusing on technology, innovation, strategic planning, change management, and the setup of new capabilities.
Patrick is a Society of Clinical data Management board member and leads the SCDM innovation committee which recently released 3 reflection papers on the evolution of Clinical Data Management toward Clinical Data Science.
Partner for this event
endpoint
Endpoint Clinical is an interactive response technology (IRT) systems and solutions provider that supports the life sciences industry. We deliver innovative and high-quality clinical trial management technology. Our fully customizable randomization and trial supply management (RTSM) solutions are backed by over a decade of award-winning experience and expertise. Built on client insight, collaboration and ingenuity, Endpoint RTSM solutions ensure that our clients can focus on the science of developing lifesaving medicines.
With over 600 team members globally and offices across the US, EU and Asia, Endpoint is headquartered in Wakefield, Massachusetts.
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