Human tissue biobanking encompasses a wide range of activities and study designs and is critical for application of a wide range of new technologies (-"omics") to the discovery of molecular patterns of disease and for implementation of novel biomarkers into clinical trials. Pathology is the cornerstone of hospital-based tissue biobanking. Pathologists not only provide essential information identifying the specimen but also make decisions on what should be biobanked, making sure that the timing of all operations is consistent with both the requirements of clinical diagnosis and the optimal preservation of biological products. This document summarizes the conclusions of a Pathology Expert Group Meeting within the European Biological and Biomolecular Research Infrastructure (BBMRI) Program. These recommendations are aimed at providing guidance for pathologists as well as for institutions hosting biobanks on how to better integrate and support pathological activities within the framework of biobanks that fulfill international standards.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2852521 | PMC |
http://dx.doi.org/10.1007/s00428-010-0887-7 | DOI Listing |
China CDC Wkly
December 2024
Global Health Institute, School of Public Health, Xi'an Jiaotong University Health Science Center, Xi'an City, Shaanxi Province, China.
China faces a critical public health challenge with obesity rates exceeding 50% among adults and 20% among children. In response, the National Health Commission launched a comprehensive three-year "Year of Weight Management" initiative in March 2024, further emphasized by the 36th Patriotic Health Month's theme "Healthy Towns - Healthy Weight" in April 2024. These initiatives underscore the urgent necessity for implementing comprehensive strategies to combat obesity and its associated non-communicable diseases.
View Article and Find Full Text PDFZhongguo Yi Liao Qi Xie Za Zhi
September 2021
The automatic diagnosis function of the electrocardiograph (ECG) machine directly affects the clinical application of the device. However, there is currently no unified criteria for the evaluation of the automatic diagnosis function of the 12-lead ECG machine in clinic. We established a 12-lead ECG automatic diagnostic function clinical evaluation specification from the scope of the specification, the automatic diagnostic function judgment rules, general technical measurement requirements, test methods and conditions, and ECG data input.
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