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Sorcero AI Platform™ Accelerates Medical Affairs Teams Ability to Improve Patient Outcomes with Medically-tuned Generative AI

Sorcero AI Platform™ Accelerates Medical Affairs Teams Ability to Improve Patient Outcomes with Medically-tuned Generative AI
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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 statesDeborah collyarCatina olearyClinical trials expert groupDevelopment of duchenne video assessmentEuropean parliamentDrug administrationDrug developmentPatient advocates in researchUs national library of medicineHealth literacy mediaEuropean unionEuropean medicines agencyNational academies of sciencesNational academiesMat stevens

Ethical Considerations for the Inclusion of Patient-Reported Outcomes in Clinical Research

These international, consensus-based, patient-reported outcomes (PRO)–specific guidelines aim to lay out the ethical considerations that researchers, research e

Eteläuomen läiUnited kingdomWest midlandsUnited kingdom generalAmanda hunnDaiichi sankyoHaf daviesMelaniej calvertCruz riveraResearch council experimental medicineNipro corpJapan media corpLanguage summaries for the research participantsInternational delphiBirmingham health partners centre for regulatory scienceBirmingham biomedical research centre

Considerations For Creating Plain Language Summaries

Advance planning is the key to streamlining plain language summaries (PLS). With the EMA’s new Clinical Trial Information System (CTIS) on.

United kingdomDarcy grabensteinCourtneay parsonsEuropean medical writers associationEuropean medicines agencyUnited kingdom health research authoritySenior managerContent strategyClinical trial information systemEuropean clinical trial regulationHealth research authorityPlain language summaries

Communicating for change – creating effective medical communications

Communicating for change – creating effective medical communications
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