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21 CFR 610.67 - Bar code label requirements.

There are 2 Updates appearing in the Federal Register for 21 CFR 610. Select the tab below to view, or View eCFR (GPOAccess)
§ 610.67
Bar code label requirements.
Biological products must comply with the bar code requirements at § 201.25 of this chapter. However, the bar code requirements do not apply to devices regulated by the Center for Biologics Evaluation and Research or to blood and blood components intended for transfusion. For blood and blood components intended for transfusion, the requirements at § 606.121(c)(13) of this chapter apply instead.
[69 FR 9171, Feb. 26, 2004]

Title 21 published on 2012-04-01

The following are only the Rules published in the Federal Register after the published date of Title 21.

For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.

  • 2012-05-24; vol. 77 # 101 - Thursday, May 24, 2012
    1. 77 FR 30887 - Amendments to Sterility Test Requirements for Biological Products; Correction
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule, correction.
      Effective June 4, 2012.
      21 CFR Parts 600, 610, and 680

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


United States Code
USC : Title 21 - FOOD AND DRUGS

§ 360c - Classification of devices intended for human use

§ 360d - Performance standards

§ 360h - Notification and other remedies

§ 360i - Records and reports on devices

§ 371 - Regulations and hearings

§ 372 - Examinations and investigations

U.S.C. : Title 42 - THE PUBLIC HEALTH AND WELFARE

§ 263 - Preparation of biological products by Service

§ 263a - Certification of laboratories

Title 21 published on 2012-04-01

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 610 after this date.

  • 2012-05-24; vol. 77 # 101 - Thursday, May 24, 2012
    1. 77 FR 30887 - Amendments to Sterility Test Requirements for Biological Products; Correction
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule, correction.
      Effective June 4, 2012.
      21 CFR Parts 600, 610, and 680