This week's FierceBiotech is brought to you by Rho.

5469c2bcec492af9843284ede37d6326.jpg

Hi Colleague,

Does the time between a patient’s data being entered at a visit to showing up in a table in the clinical study report seem a bit mysterious to you? Do all of the acronyms used in data standards blur together? In this presentation, Principal Statistical Scientist Ben Vaughn demystifies the process of moving clinical trial data from collection in the case report form to presentation to the FDA.

Topics covered in this presentation include:

  • A high-level overview of what statisticians do with clinical trial data
  • Connecting the dots between the time data are entered in a CRF to the point where they are submitted to the FDA
  • How CDISC data standards (CDASH, SDTM, and ADaM) fit in

View Presentation

Want to reach 150,000+ FierceBiotech subscribers with your own message?
Contact aalcover@fiercemarkets.com or call 202-824-5074.



About this email: In order to receive FierceBiotech for free, we ask that you accept an occasional email promotion from our sponsors. We carefully screen each promotion and never sell or give away your personal information. If you do not want to receive these messages, you can unsubscribe entirely from FierceBiotech.
Click here to unsubscribe. Refer to our Privacy Policy.

FierceMarkets, a division of Questex, LLC
1900 L St. NW Suite 400 
Washington, DC 20036

.