# S4A Duration of Chronic Toxicity Testing in Animals (Rodent and Nonrodent Toxicity Testing) - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/s4a-duration-of-chronic-toxicity-testing-in-animals-rodent-and-nonrodent-toxicity-testing/274c345e-d541-42de-a26c-85fefde1aa9e > FDA guidance document: S4A Duration of Chronic Toxicity Testing in Animals (Rodent and Nonrodent Toxicity Testing). Issue date: June 25, 1999. Get complete insights and analysis. --- ## Details - Title: S4A Duration of Chronic Toxicity Testing in Animals (Rodent and Nonrodent Toxicity Testing) - Communication Type: Guidance Document - Product Type: drugs - Office Name: Center for Drug Evaluation and Research - Office URL: /offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c - Issue Date: 1999-06-25 - Last Changed: 2020-05-06 - Docket Number: FDA-1997-D-0153 ## Related Documents - [Single Dose Acute Toxicity Testing for Pharmaceuticals](https://www.globalkeysolutions.net/guidances/guidance-document/single-dose-acute-toxicity-testing-for-pharmaceuticals/daee90ca-d341-46e0-9470-bbd8b5c640c8) - [Protection of Human Subjects: Categories of Research That May Be Reviewed by the Institutional Review Board (IRB) Through an Expedited Review Procedure: Guidance for Institutional Review Boards and Clinical Investigators](https://www.globalkeysolutions.net/guidances/guidance-document/protection-of-human-subjects-categories-of-research-that-may-be-reviewed-by-the-institutional-review-board-irb-through-an-expedited-review-procedure-guidance-for-institutional-review-boards-and-clinical-investigators/3f36bd8c-c7f3-43b6-8b85-5e6e92984169) - [Q2(R1) Validation of Analytical Procedures: Text and Methodology Guidance for Industry: Guidance for Industry](https://www.globalkeysolutions.net/guidances/guidance-document/q2r1-validation-of-analytical-procedures-text-and-methodology-guidance-for-industry-guidance-for-industry/8d826e71-f7db-43f1-b28a-787f4e374c57)