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...
Source: clinicalleader.com
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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
Source: jamanetwork.com
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...
Source: clinicalleader.com
Communicators: Morgan C. Hill
Communicators: Morgan C. Hill by What inspires you to succeed in your role at ICON? The impact we can have on patients’ lives is incredibly inspiring – we are the communicators who can convey the value of a therapy by translating raw data around patient outcomes into an easily digestible, at-a-glance snapshot of overall patient experience before- versus after-therapy. We decipher thousands of pages of clinical trial data into a comprehensive story of how, why and how much relief a particular therapy can bring to patients. In doing this, we are extremely fortunate to collaborate with some ...
Source: pharmatimes.com