CLSI AUTO12
Specimen Labels: Content and Location, Fonts, and Label Orientation
Minimize specimen mislabeling and enhance patient safety with CLSI document AUTO12. This standard provides clear guidelines for specimen label content, format, and orientation. It defines consistent label dimensions (2 × 1 inches), specifies the exact placement of patient information, and establishes rules for truncation, barcode positioning, and font size to improve readability and scanning accuracy. By implementing CLSI AUTO12, laboratories can reduce human errors, streamline workflows, and improve specimen traceability, ensuring accurate identification and reliable results.
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{{FormatPrice(nonMemberPrice)}} List PriceClinical and Laboratory Standards Institute document AUTO12-A—Specimen Labels: Content and Location, Fonts, and Label Orientation; Approved Standard was developed to reduce the unacceptably high incidence of mislabeled specimens in clinical laboratories. The standard specifies locations and formats for the required human-readable elements that must appear on the label for each clinical laboratory specimen (except labels with limited space, eg, slides and pediatric specimens), a standard label size of 2 × 1 inches (50.8 × 25.4 mm), and an exact required location and format on this label for other commonly used elements. The patient’s name is judged to be the single most important element in correct specimen identification and is always to be in the top left corner on each label. The standard also specifies rules for truncation for long patient names, the location and size of the bar code on each label, a list of the most commonly used variable elements that can appear on specimen labels, and the required orientation of labels on specimen tubes.
This document presents a standard for specimen label content, format, and placement. This document is intended for health care providers; laboratory information system (LIS) vendors, diagnostic vendors, and vendors that manufacture labels and/or label printers; and for all other entities that collect, prepare, or handle patient specimens and must use, print, or read specimen labels. With some exceptions, such as slides and pediatric specimens that have limited label space, this standard is applicable to all laboratory specimens from the point of collection, including all transfers of specimens from one provider to another.
The scope is limited, as described in Sections 1.1 to 1.7, to reduce complexity in both developing and implementing the standard.
The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus standard for use in satisfying a regulatory requirement.
This document is available in electronic format only.
Clinical and Laboratory Standards Institute document AUTO12-A—Specimen Labels: Content and Location, Fonts, and Label Orientation; Approved Standard was developed to reduce the unacceptably high incidence of mislabeled specimens in clinical laboratories. The standard specifies locations and formats for the required human-readable elements that must appear on the label for each clinical laboratory specimen (except labels with limited space, eg, slides and pediatric specimens), a standard label size of 2 × 1 inches (50.8 × 25.4 mm), and an exact required location and format on this label for other commonly used elements. The patient’s name is judged to be the single most important element in correct specimen identification and is always to be in the top left corner on each label. The standard also specifies rules for truncation for long patient names, the location and size of the bar code on each label, a list of the most commonly used variable elements that can appear on specimen labels, and the required orientation of labels on specimen tubes.
This document presents a standard for specimen label content, format, and placement. This document is intended for health care providers; laboratory information system (LIS) vendors, diagnostic vendors, and vendors that manufacture labels and/or label printers; and for all other entities that collect, prepare, or handle patient specimens and must use, print, or read specimen labels. With some exceptions, such as slides and pediatric specimens that have limited label space, this standard is applicable to all laboratory specimens from the point of collection, including all transfers of specimens from one provider to another.
The scope is limited, as described in Sections 1.1 to 1.7, to reduce complexity in both developing and implementing the standard.
The U.S. Food and Drug Administration (FDA) has evaluated and recognized this approved-level consensus standard for use in satisfying a regulatory requirement.
This document is available in electronic format only.