A standardized document, typically in a portable document format, communicates the outcome of a laboratory analysis conducted to detect the presence of specified substances within a biological sample. This document generally includes identifying information about the individual tested, the testing facility, the date of the test, and a list of substances screened, along with their corresponding results, which may be positive, negative, or require further evaluation. For example, a company might use this document to verify an employee’s compliance with a substance abuse policy.
The value of such a report lies in its provision of a verifiable record for compliance, legal, or medical purposes. Historically, these records were often maintained physically; however, their digital format offers improved accessibility, secure storage, and efficient distribution. The use of a universally readable digital format ensures compatibility across various computer systems and facilitates easy sharing among authorized parties, such as employers, medical professionals, or legal representatives. This accessibility is crucial in time-sensitive situations where rapid verification of results is required.
