Join the Clymb Team at PHUSE US Connect 2025!

Be part of the future of pharmaceutical research and development with the Clymb Clinical team at the PHUSE US Connect 2025. This event is a premier gathering for professionals in data science, clinical development, and regulatory standards, designed to inspire innovation and collaboration across the pharmaceutical industry.

Event highlights

Explore a rich agenda filled with cutting-edge presentations, hands-on workshops, and interactive sessions covering topics such as data standards, regulatory compliance, statistical analysis, and the latest advancements in technology. Whether you’re a seasoned expert or just starting your career, PHUSE US Connect 2025 offers a platform for growth, learning, and networking. This year, 7 members of the Clymb Clinical team will be attending the event, showcasing their thought leadership through 6 paper presentations across the team.

Visit our booth

Stop by our booth #35 to meet the Clymb Clinical team, discuss your data needs, and discover how our innovative solutions can support your clinical development goals. Our team is eager to answer your questions and explore potential partnerships.

Check out our Paper Presentations at the event!

1. Paper Presentation:

Title: The Development of the CDISC eTFL Portal to Support the Adoption and Implementation of the Analysis Result Standard

Presenters: Bhavin Busa and Bess LeRoy

Attend this session to learn about the development and implementation of the CDISC eTFL portal.

2. Paper Presentation:

Title: Let the Machine Do the Coding: A SAS-based Framework for Automating TFL Generation with ARS Metadata

Presenter: Julie Wachara

Explore how automation streamlines the programming workflow with a SAS-based framework
leveraging TFL shells and CDISC ARS metadata. This session highlights
metadata-driven solutions that optimize programming tasks, reduce manual
effort, and ensure adaptability in dynamic clinical trial environments.

3. Paper Presentation:

Title: Towards TFL Automation: A Meta-Programming Approach in R Using ARS

Presenter: Malan Bosman

Join this session to learn about “Siera,” an innovative R package that leverages CDISC’s Analysis Results Standard (ARS) to advance TFL automation. Discover how meta-programming in R can bridge the gap in automating Analysis Results while enabling flexibility and transparency through open-source technologies.

4. Paper Presentation:

Title: Gen-AI for Statistical Reporting and CSR Writing: Leveraging CDISC ARS Model

Presenter: Navin Dedhia

Explore the future of Clinical Study Report (CSR) writing with a Gen-AI-driven model that harnesses the power of CDISC’s ARS and ARD metadata. Attend this session to learn how this cutting-edge approach automates narrative summaries, streamlines reporting processes, and enhances efficiency for medical writers, clinicians, and biostatisticians.

5. Paper Presentation:

Title: Selecting GeARS: Analysis Results Standard Implementation Options for Accelerated Analysis and TFL Automation

Presenter: Richard Marshall

Discover how the Analysis Results Standard (ARS) enables different implementation strategies for automating analyses and TFL generation. Attend this session to explore ARS metadata interpretation, reverse compatibility with macro libraries, and leveraging vendor-neutral, software-agnostic attributes for streamlined workflows.

6. Paper Presentation:

Title: Introducing TFL Viewer: A Centralized Platform for TFL Review, Collaboration and Approval

Presenter: Bhavin Busa

Learn how TFL Viewer streamlines TFL review, feedback, and approval, enhancing collaboration and accelerating clinical trial workflows.