part_subject: "GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES"
subpart_code: "F"
subpart_subject: "Test and Control Articles"
section_number: "58.107"
section_subject: "Test and control article handling."
cfr_reference: "21 CFR 58.107"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 1 to 99"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
---
Procedures shall be established for a system for the handling of the test and control articles to ensure that:
(b)Distribution is made in a manner designed to preclude the possibility of contamination, deterioration, or damage.
(c)Proper identification is maintained throughout the distribution process.
(d)The receipt and distribution of each batch is documented. Such documentation shall include the date and quantity of each batch distributed or returned.