May 15, 2017
What's NewThe Clinical Trials Transformation Initiative (CTTI) is hosting a special webinar in which it will unveil new recommendations for registry assessment and design that can assist in making embedded clinical trials suitable for regulatory purposes. The presenters of the webinar will be:
John Laschinger, MD, Medical Officer, Center for Devices and Radiological Health, U.S. FDA, and
Jules Mitchel, MBA, PhD, President, Target Health Inc.
Here are the details:
Title: CTTI Recommendations from the Registry Trials ProjectDate: May 18, 2017 12:00-1:00 p.m. ET (GMT-05:00) Webinar Link: When it's time, Join the Meeting
The webinar will include the following practical, evidence-based strategies:
How to assess the reliability, relevance, and robustness of registry data
How to assure patient protections
How to make modifications needed to accommodate research needs
For more information about Target Health contact Warren Pearlson (212-681-2100 ext. 165). For additional information about software tools for paperless clinical trials, please also feel free to contact Dr. Jules T. Mitchel. The Target Health software tools are designed to partner with both CROs and Sponsors.
Joyce Hays, Founder and Editor in Chief of On Target
Jules Mitchel, Editor