GLSP Webinar
Enhancing transparency and trust in clinical trials: GLSP’s recommendations for effective lay protocol synopses
Description
The Lay Protocol Synopsis (LPS) plays a key role in making clinical trials understandable to everyone. Recommended under the EU Clinical Trial Regulation, this short document translates complex protocol information into clear, accessible language for the wider public. Over the past two years, an international expert group has developed detailed recommendations for writing effective LPS documents. Following a global consultation—with nearly 70 contributors providing more than 400 comments—the guidance has now been refined and finalised.
Join our webinar to explore the final recommendations, gain insights from the expert group, and take part in an open exchange with the community.
Programme
| 14:00 |
Welcome and Introduction |
| 14:05 |
General introduction: structure of the recopmmendation document, objective of guideline, ethics, Category I inclusion, referencing other documents, “LPS as part of lay documents” |
| 14:17 |
Target audience |
| 14:27 |
Length, translations, redactions, specialised terms and abbreviations, glossary |
| 14:39 |
Layout and graphics |
| 14:51 |
Order: ordering of topics, title and its location, headings as questions, proposed structure |
| 15:03 |
Objective and rationale, endpoints (primary, secondary) |
| 15:13 |
Specific recommendations (all those that have not been covered before) |
| 15:30 |
Open Discussion |
| 16:00 |
End of Webinar |