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The Minnesota Public Interest Research Group (also known as MPIRG) describes itself as "a grassroots, non-partisan, nonprofit, student-directed organization that empowers and trains students and engages the community to take collective action in the public interest throughout the state of Minnesota."
Polymeric immunoglobulin receptor (pIgR) is a transmembrane protein that in humans is encoded by the PIGR gene. [5] It is an Fc receptor which facilitates the transcytosis of the soluble polymeric isoforms of immunoglobulin A and immunoglobulin M (pIg) and immune complexes. pIgRs are mainly located on the epithelial lining of mucosal surfaces of the gastrointestinal tract.
Massachusetts Public Interest Research Group (MASSPIRG) is a non-profit organization that is one of the largest of the state PIRG organizations. It works on a variety of political activities, including textbook trading on college campuses.
Plates vi & vii of the Edwin Smith Papyrus (around the 17th century BC), among the earliest medical guidelines. A medical guideline (also called a clinical guideline, standard treatment guideline, or clinical practice guideline) is a document with the aim of guiding decisions and criteria regarding diagnosis, management, and treatment in specific areas of healthcare.
The WHO Smart Guidelines are part of a broader global trend of digitizing clinical guidelines to make them more actionable in healthcare systems. For example, the Centers for Disease Control and Prevention (CDC) in the United States developed the "Adapting Clinical Guidelines for the Digital Age" (ACG) initiative, which promotes a holistic ...
A Guideline Comparison utility that gives users the ability to generate side-by-side comparisons for any combination of two or more guidelines; Guideline Syntheses prepared by NGC staff, comparing guidelines covering similar topics, highlighting areas of similarity and difference.
In drug development and medical device development [1] the Investigator's Brochure (IB) is a comprehensive document summarizing the body of information about an investigational product ("IP" or "study drug") obtained during a drug trial.
In the guideline document, EMA inspectors state that paper TMF documents may be stored in electronic eTMF systems, and after this process, that the paper may be destroyed. The use of eTMF systems for electronic storage is fully supported by the EMA in clinical trials as a replacement for paper.