21 CFR 610, Subpart E - Testing Requirements for Communicable Disease Agents
- § 610.40 — Test requirements.
- § 610.41 — Donor deferral.
- § 610.42 — Restrictions on use for further manufacture of medical devices.
- § 610.44 — Use of reference panels by manufacturers of test kits.
- § 610.46 — Human immunodeficiency virus (HIV) “lookback” requirements.
- § 610.47 — Hepatitis C virus (HCV) “lookback” requirements.
- § 610.48 — Hepatitis C virus (HCV) “lookback” requirements based on review of historical testing records.
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.
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.
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.
