Managing External Data Sources in Clinical Trials: Current and Future Strategies, Upcoming Webinar Hosted by Xtalks

TORONTO, Sept. 16, 2020 /PRNewswire-PRWeb/ -- As clinical trials are incorporating an increasing number of sources of non-case-report-form (CRF) data from wearable devices and various laboratories, management of clinical data must address larger, disparate volumes of external data sources.

Metadata

Provider:

PR Newswire

Retrieved on:

Wednesday, September 16, 2020

Information

Tags:

Clinical research, Health, Medical research, Clinical data management, Case report form, Pharmaceutical industry, Food and Drug Administration, Clinical trial

Geotags:

ONTARIO

Organisation:

XTALKS

Website:

http://xtalks.com

Summary

Key Points:

TORONTO, Sept. 16, 2020 /PRNewswire-PRWeb/ -- As clinical trials are incorporating an increasing number of sources of non-case-report-form (CRF) data from wearable devices and various laboratories, management of clinical data must address larger, disparate volumes of external data sources.
These non-CRF clinical data can cause delays in resolving queries and can place additional burden on eCRF data managers.
In this webinar, our thought leaders discuss best practices for dealing with these complex data structures and implementing a data strategy that not only addresses needs for today, but also explores future tactics for proactively optimizing management of external data sources.
For more information or to register for this event, visit Managing External Data Sources in Clinical Trials: Current and Future Strategies .

Managing External Data Sources in Clinical Trials: Current and Future Strategies, Upcoming Webinar Hosted by Xtalks

TORONTO, Sept. 16, 2020 /PRNewswire-PRWeb/ -- As clinical trials are incorporating an increasing number of sources of non-case-report-form (CRF) data from wearable devices and various laboratories, management of clinical data must address larger, disparate volumes of external data sources. These non-CRF clinical data can cause delays in resolving queries and can place additional burden on eCRF data managers.

Efficiently managing this level of complexity and avoiding delays in reaching database lock requires a strategic approach that can track, QC, reconcile and ensure the veracity of a rapid inflow of non-CRF data.

In this webinar, our thought leaders discuss best practices for dealing with these complex data structures and implementing a data strategy that not only addresses needs for today, but also explores future tactics for proactively optimizing management of external data sources.

Join Arshad Mohammed, MBBS, Global Head CDM, Covance FSPx and David Howard, BSC(Hons), Global Head of External and Clinical Data Strategy, Covance FSPx, for the live webinar on Tuesday, September 29, 2020 at 10am EDT (3pm BST/UK).

For more information or to register for this event, visit Managing External Data Sources in Clinical Trials: Current and Future Strategies.

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/

SOURCE Xtalks