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Results of the present study contribute to this standardization and validation process in the ram.
While software solutions for metagenomics proliferate, integration of metagenomics in clinical care requires method standardization and validation.
Here, we critically review progress towards standardization and validation of methods used to characterize manufactured nanomaterials to assess their health and safety risks.
A crucial milestone towards the standardization and validation of time motion studies corresponds to a common understanding, accompanied by a proper recognition of the distinct techniques it encompasses.
Translating a new technology from the research to clinical domain however first requires standardization and validation.
Without such standardization and validation of biomarkers, valuable research resources are being squandered, because reported results cannot be translated into the desired clinical use and patient outcomes.
In addition to technology stability (robustness), non-invasiveness, and broad availability, there are two main prerequisites for the effective use of imaging biomarkers, which are standardization and validation.
In comparison, as an in-house developed method, KRAS-TMGB is of low cost but it requires additional lab expertise and efforts for standardization and validation.
Standardization and validation methods have been developed [ 12– 15].
The Swedish standardization and validation is based on Hansson and Olsson [ 25].
Even so, further standardization and validation are required before clinical trials are set in motion.
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