January 21-22, 2018

Our team of public health and clinical experts have been meeting to finalise the content that will be on the App we're developing. This App is intended for the description and coding of birth defects in areas and regions of low-resources.

The goal is to build greater capacity and mainstream the surveillance of birth defects in health systems. These experts come from around the world, including Latin America, North America, Europe, Africa, and Southeast Asia.

Meeting of The International Committee for Congenital Anomaly Surveillance Tools

Pictured above (back row, L-R): Lorenzo Botto, Ester Garne, Lewis Holmes, Linda Barlow and seated (L-R): Christine Halleux, Shana Godfred Cato, Helen Dolk, Pilar Guatibonza.  Joining remotely: Cindy Moore, Priya Karna, and Leke Aminkeng.