How to Shorten Clinical Database Builds by 60%

Clinical Trials, Life Sciences,
  • Tuesday, July 16, 2019

Despite the promise of enhanced efficiency with electronic data capture (EDC) systems, life sciences companies are not seeing real improvement. Rather, they are cutting weeks off their database build times by taking a whole new approach to data management.

Too often, EDC systems limit this kind of change. But with an agile EDC, companies are using spec-less design, risk-based UAT, and live UAT roundtables to shorten the database build process by 40-60%.

In this free webinar, data management experts will show participants how technology can enable these changes and illustrate what teams can do right now to start seeing improvements.

Speakers

http://Hugo%20Cervantes,%20Vault%20CDMS%20Strategy

Hugo Cervantes, Vice President, Vault CDMS Strategy

Hugo Cervantes is responsible for Vault EDC strategy, market adoption and customer engagement. Hugo has spent the last 15 years in management consulting and professional services, helping biopharmaceutical organizations increase their productivity, innovate and grow.

Message Presenter

Dan Crawford, Senior Director, Vault CDMS Strategy

Dan Crawford has worked in the pharmaceutical industry for more than 25 years. He has participated in or had oversight for hundreds of clinical trials across various therapeutic areas.

Dan is a member of the CDISC-CDASH core team and CDASH CFAST Expanded Leadership Team. In addition, he has performed clinical assessments to assess compliance and provide oversight on adherence to SDTM standards/FDA submissions. Currently Dan is senior director, CDMS strategy where he is responsible for growing CDMS in the CRO space.

Message Presenter

Who Should Attend?

This webinar will appeal to senior professionals in the areas of:

  • Clinical Data Management
  • Data Management
  • Data Science
  • Clinical Science
  • Clinical Development
  • Biometrics
  • Informatics

What You Will Learn

In this free webinar, attendees will gain insights on:

  • Current trends in clinical data management
  • Best practices for speeding study timelines
  • How modern EDC enables greater trial efficiency

Xtalks Partner

Veeva Systems

Veeva Systems Inc. is a leader in cloud-based software for the global life sciences industry. Committed to innovation, product excellence, and customer success, Veeva has more than 700 customers, ranging from the world’s largest pharmaceutical companies to emerging biotechs. Veeva is headquartered in the San Francisco Bay Area, with offices throughout North America, Europe, Asia, and Latin America. For more information, visit veeva.com.

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