CFR — Code of Federal Regulations Title 21 Part 211 Subpart E — Control of Components and Drug Product Containers and Closures § 211.89 — Rejected components, drug product containers, and closures.

[Code of Federal Regulations]
[Title 21, Volume 4]
[CITE: 21CFR211.89]

TITLE 21–FOOD AND DRUGS
CHAPTER I–FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER C – DRUGS: GENERAL
PART 211 — CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS

Subpart E – Control of Components and Drug Product Containers and Closures

Sec. 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.

As per US Health & Human Services, the information on this page is current as of Mar. 22, 2024.