non-series-jmp-data-banner.png
Live Webinar

Streamlining clinical trial review, analysis, and reporting with JMP Clinical

Date: 10 October 2024
Time: 14:00 CEST I 13:00 BST 
Location: Online
Duration: 1 hour
Registration: Free

Clinical trials are inherently complex, and in today’s pharmaceutical and biologics landscape, efficiency, cost savings, data management, data volume, and adherence to stringent regulatory requirements are critical challenges. To address these challenges, study teams need ongoing access to tools that allow them to monitor their data interactively and graphically to assess data quality and patient safety. To develop a more complete picture of a novel treatment in the context of current regulatory trends, these same tools should empower the study team to quickly and easily gain additional insight for key data beyond the deliverables programmed to complete study reports.

Join Richard Zink and Valérie Nedbal on Oct. 10 to discover how JMP Clinical, a specialized clinical data analysis software, can enhance your company’s capabilities in clinical trial review, analysis, and reporting. Designed specifically for clinical trial data, JMP Clinical is a ready-to-use, interactive and visual software that offers tools to:

  • Explore trends and relationships.
  • Identify safety and data integrity issues.
  • Perform medical monitoring.
  • Produce customized patient profiles and adverse event narratives.
  • Enrich data monitoring committee meetings.
  • Conduct advanced statistical analysis.

JMP Clinical empowers  the study team to make informed decisions throughout the trial life cycle, helping you bring your innovations to market faster, with more confidence - and greater insight - than ever before.

Who should attend: Medical monitors, medical writers, data managers, and clinical operations personnel working in areas such as adverse event/concomitant medications/labs reporting, risk-based monitoring, and data quality/fraud detection.

 


Richard C. Zink
Speaker

Richard C. Zink

Principal Reseach Fellow, JMP Statistical Discovery

Richard C. Zink is Principal Research Fellow at JMP Statistical Discovery and has spent 20+ years in and around clinical trials and medical product development. Richard is Associate Editor for the DIA journal Therapeutic Innovation & Regulatory Science and is author, editor, and contributor to 9 books on statistical topics in clinical trials and clinical research.  He holds a Ph.D. in Biostatistics from the University of North Carolina at Chapel Hill, where he serves as Adjunct Professor of Biostatistics. Richard was awarded the distinction of Fellow of the American Statistical Association in 2020.

 


Valérie Nedbal, JMP
Speaker

Valérie Nedbal

JMP Senior Systems Engineer, Global Enablement

Valérie Nedbal, PhD, serves as Senior System Engineer in the Global Technical Enablement Team at JMP Statistical Discovery LLC in Heidelberg, working closely with customers for software knowledge and implementation.

Prior to joining JMP, Valérie was product manager for bioinformatics for SAS EMEA and supported life sciences sales activities. Before joining SAS, Valérie was Senior Field Marketing Manager for LION bioscience AG, a software company offering solutions in the Life Science Market.


Register now to attend online

*
*
*
 
*
*
*
*
  Please subscribe me to JMP Newswire, the monthly newsletter for JMP users.
  Yes, you may send me emails occasionally about JMP products and services. I understand that I can withdraw my consent at any time by clicking the opt-out link in the emails.

JMP Statistical Discovery LLC. Your information will be handled in accordance with our Privacy Statement.