The laboratory shall provide pre-collection information and instructions detailed enough to protect sample integrity: patient preparation, type and amount of sample with containers, additives and collection order, special timing, clinical information affecting collection, examination or interpretation, labelling for unequivocal patient identification and sample source and site including multiple samples, tissue pieces and slides, and the acceptance and rejection criteria specific to the examinations.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.