In this free webinar, learn about the Clinical Data Interchange Standards Consortium (CDISC), and how to adopt and use CDISC standards. Attendees will get guidance from the organization that sets the standards. The featured speakers will discuss how technology can help with CDISC compliance and standardization.
TORONTO, Oct. 25, 2022 /PRNewswire-PRWeb/ -- The Clinical Data Interchange Standards Consortium (CDISC) compliance is now mandatory for clinical trial submissions to the US Food and Drug Administration (FDA) and Pharmaceuticals and Medical Devices Agency (PMDA). And for many academic institutions, this is now a condition of their grant funding. However, adopting CDISC standards isn't just a necessity. It's an important investment that enables more meaningful research, and easier data analysis, with deeper insights.
In addition, those who take steps to implement standards benefit from reuse. Rather than designing new studies from scratch, content can be reused across future studies and standards, enabling significant time and resource efficiencies.
Attendees will hear how the University of Alabama (UAB) and the University of Utah are tackling CDISC compliance and embracing the benefits of standardization. Experts from both universities will tell the story of their compliance journey — their starting point; what they were looking to achieve; what they needed help with; the challenges they faced; what they achieved; and future aspirations.
Attendees will have the opportunity to ask questions specifically related to their own organizational projects or specific challenges, and how best to address them.
Register to learn about the need for standardization and hear from CDISC themselves, including their guidance and approach to standards adoption.
Join Coretta (Thomas) Robinson, Program Manager, The University of Alabama (UAB); Russ Telford, Director of Biostatistics and Clinical Data Management, The University of Utah; Ed Chappell, Solutions Consultant, Formedix; and Mark Wheeldon, CEO, Formedix, for the live webinar on Tuesday, November 8, 2022, at 1pm EST (10am PST).
For more information, or to register for this event, visit The Need for Standardization and CDISC: Insights from The University of Alabama, The University of Utah & CDISC.
ABOUT XTALKS
Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.
To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/
Contact:
Vera Kovacevic
Tel: +1 (416) 977-6555 x371
Email: [email protected]
ABOUT FORMEDIX
Formedix is a specialist developer of a clinical metadata repository (CMDR) and study automation platform, designed to enable the rapid set-up of clinical trials, in compliance with the requirements of the Clinical Data Interchange Standards Consortium (CDISC).
The company has more than two decades of experience in CDISC standards development and has contributed to the creation of the CDISC ODM, Define and Dataset-XML models. Formedix is on the CDISC Data Exchange Standards team and its clinical MDR is currently being used by the organization to design and manage their CDASH eCRF standards.
For more information, please visit http://www.formedix.com.
Media Contact
Vera Kovacevic, Xtalks, +1 (416) 977-6555 x371, [email protected]
SOURCE Xtalks
Share this article