Idaho § 56-2304 GENERAL REQUIREMENTS

Idaho Statutes

§ 56-2304 — GENERAL REQUIREMENTS

Idaho § 56-2304

Title 56PUBLIC ASSISTANCE AND WELFARE

Ch. 23QUALITY ASSURANCE FOR CLINICAL LABORATORIES

This text of Idaho § 56-2304 (GENERAL REQUIREMENTS) is published on Counsel Stack Legal Research, covering Idaho primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

Idaho Code § 56-2304 (2026).

Text

(1)A clinical laboratory shall have adequate space, equipment, and supplies to perform the services offered by the laboratory with accuracy, precision, and safety.

(2)Practitioners legally authorized to diagnose, treat, and prescribe are authorized to order both waived and nonwaived tests and receive results. Laboratory directors are authorized to order the waived tests listed on an approved registration form and receive results.

(3)Clinical laboratories shall satisfactorily participate in proficiency testing programs approved by the department of health and welfare and ensure all proficiency testing results are available to the department.

(4)Clinical laboratories shall:

(a)Identify the person responsible for performing a procedure;

(b)Maintain testing records for at least two (2) y

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(1) A clinical laboratory shall have adequate space, equipment, and supplies to perform the services offered by the laboratory with accuracy, precision, and safety.
(2) Practitioners legally authorized to diagnose, treat, and prescribe are authorized to order both waived and nonwaived tests and receive results. Laboratory directors are authorized to order the waived tests listed on an approved registration form and receive results.
(3) Clinical laboratories shall satisfactorily participate in proficiency testing programs approved by the department of health and welfare and ensure all proficiency testing results are available to the department.
(4) Clinical laboratories shall:
(a) Identify the person responsible for performing a procedure;
(b) Maintain testing records for at least two (2) years and ensure that test reports are readily accessible upon request; and
(c) Identify specimens referred to other certified laboratories and identify the reference laboratory by name and address.