Keep up to date with the latest developments at CDISC and follow our news feeds!
14 Oct 2016

Despite considerable potential benefits from using common standards for collecting and reporting information from clinical trials, research sponsors and investigators have been slow to move in this direction. That appears to be changing as the December 2016 deadline looms for meeting the FDA requirement that all applications for new drugs and biologics compile and submit clinical trial data electronically and according to standardized format.

13 Oct 2016

CDISC conducted a series of Listening Tour teleconferences to hear from our member companies about the challenges and opportunities they face in implementing CDISC standards. This paper presents the results.

23 Sep 2016

Austin, TX – 23 September 2016 – The Clinical Data Interchange Standards Consortium (CDISC) and Cohen Veterans Bioscience today announced a collaboration to establish a new CDISC Therapeutic Area Data Standard for post-traumatic stress disorder (PTSD).

Approximately 7 to 8 out of every 100 people will experience PTSD at some point during their lives and about 8 million adults have PTSD in a given year, according to the U.S. Department of Veterans Affairs National Center for PTSD.

20 Sep 2016

Austin, TX – 20 September 2016 – The Clinical Data Interchange Standards Consortium (CDISC) announced today that Dr. Robert Califf, FDA Commissioner, will give the opening keynote at the 2016 CDISC International Interchange at 8:00AM ET on 28 September in Bethesda, MD. Dr. Califf will expand upon the theme of the 02 August 2016 CDISC Strategy Session: “The Future of Medical Research and the Role of Standards: Forming Connections Towards Complementary Systems.”