Trial results summaries, also known as plain language summaries (PLS) or lay language summaries, convey what happened during a clinical trial in easy-to-understand language.

Best practices dictate that PLS is written at a fifth- to eighth-grade reading level. What’s more, PLS must be available in the same language as the patient’s informed consent.

In the European Union (EU), a clinical trial regulation scheduled to go into effect in mid-2020 requires all sponsors with studies in the EU to provide PLS.

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