The Clinical Trial Regulation requires the preparation of a summary of trial results in lay language.
EU Commission Recommendations exist on content of Lay Summaries but how to develop
a standard for their collaborative planning, preparation and dissemination?

Public consultation on

Good Lay Summary Practice
Recommendations prepared by the Roadmap Initiative for Good Lay Summary Practice,
with representation from over 60 international patient organisations, pharmaceutical companies, academic institutions,
not-for-profit organisations, and CROs, under the leadership of EFGCP and EFPIA.

We welcome your general and specific comments in the form available for download below, please send them via the form in WORD format to GLSP@efgcp.eu. The GLSP Document is also available for download below.

The consultation is open until 14 September 2020.