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How To Optimize Returns On Plain Language Summaries
The EMA now requires Plain Language Summaries (PLS) for clinical trials with sites in the EU. The FDA has no current regulations for PLS, but they.
United states
Deborah collyar
Catina oleary
Clinical trials expert group
Development of duchenne video assessment
European parliament
Drug administration
Drug development
Patient advocates in research
Us national library of medicine
Health literacy media
European union
European medicines agency
National academies of sciences
National academies
Mat stevens
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