Showcasing Innovation at Booth 41

Are you feeling lost on the road to automation? Visit Booth 41 at PHUSE US to meet with our experts who can assess your current state and give you a step-by-step plan for automation excellence.

Our team is dedicated to industry innovation, especially within the open source community. We endorse the use of open source programming and are actively contributing to the open source community, releasing projects that will increase efficiencies and spur further innovation across the bio-pharmaceutical industry.

Book in a meeting with one of our experts attending PHUSE US to find out how we can help with your clinical study.

Schedule a meeting

For more information on our Automation capabilities, download the brochure below.

Presentations

Stuart Malcolm, Head of Standards, Efficiency and Automation

Biomedical Concepts: What Are They and Why Should I Care?

Monday 17 March 13:30–14:00 (DS04)

Pie in the Sky or Reality? Automating the Data Flow from CDASH to TFL

Monday 17 March 16:00-17:30 (Panel Discussion)

Karen Curran, Chief Strategy Officer

Leadership in the Next Generation of Statistical Programming and Data Science
Wednesday 19 March 9:00-10:30 (Leadership Panel)

Debra Anderson, SVP, Strategic Partnerships

From Data Manager to Data Scientist: Navigating the Future of Data Management in Clinical Trials

Wednesday 19 March 11:30 – 12:00 (PD07)

Michael Byrne, Manager, Standards Programming

Next-Generation Deliverable Tracker
Wednesday 19 March 14:30 – 15:00 (SD12)

About Veramed

People. Data. Analysis. Decisions.

Veramed is a pioneering CRO redefining intelligent healthcare decision-making through end-to-end biometrics. We bring together people, innovation, and technology together with world-class governance to accelerate evidence generation and advance patient health. With skilled Statisticians, Programmers and Data Managers uniquely matched and scaled to client needs, we produce exceptional deliverables swiftly using a blend of skill, rigorous governance, and automation to optimize the speed and success of clinical research from design to submission and beyond.