Guidelines and templates for the production of summaries of clinical trial results for laypersons. These guidelines will only apply to lay summaries included in the EU database.

Owner (organization)

European Commission

Target audience

Researchers (investigators and academic researchers), Other

Types

Guidance

Formats

PDF

Levels

Unknown

Language

English

Accessibility

Easy read

Certification

No

Patients involved

No

Version date/number

26 Jan 2017

PFMD last access

28 Nov 2020

Organizations