Statutes, codes, and regulations
Code of Federal Regulations
Title 21 - FOOD AND DRUGSChapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICESSubchapter C - DRUGS: GENERALPart 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
Subpart E - CONTROL OF COMPONENTS AND DRUG PRODUCT CONTAINERS AND CLOSURES
Section 211.89 - Rejected components, drug product containers, and closures

21 C.F.R. § 211.89

Download
PDF
Current through November 30, 2024
Section 211.89 - Rejected components, drug product containers, and closures

Rejected components, drug product containers, and closures shall be identified and controlled under a quarantine system designed to prevent their use in manufacturing or processing operations for which they are unsuitable.

21 C.F.R. § 211.89