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21 CFR 1301.42 - Purpose of hearing.

§ 1301.42
Purpose of hearing.
If requested by a person entitled to a hearing, the Administrator shall hold a hearing for the purpose of receiving factual evidence regarding the issues involved in the denial, revocation, or suspension of any registration, and the granting of any application for registration to import or to manufacture in bulk a basic class of controlled substance listed in Schedule I or II. Extensive argument should not be offered into evidence but rather presented in opening or closing statements of counsel or in memoranda or proposed findings of fact and conclusions of law.
[62 FR 13956, Mar. 24, 1997]

Title 21 published on 2012-04-01

no entries appear in the Federal Register after this date.

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

§ 821 - Rules and regulations

§ 822 - Persons required to register

§ 823 - Registration requirements

§ 824 - Denial, revocation, or suspension of registration

§ 871 - Attorney General

§ 875 - Administrative hearings

§ 877 - Judicial review

§ 886a - Diversion Control Fee Account

§ 951 - Definitions

§ 952 - Importation of controlled substances

§ 953 - Exportation of controlled substances

§ 956 - Exemption authority

§ 957 - Persons required to register

§ 958 - Registration requirements

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 1301 after this date.

  • 2012-12-21; vol. 77 # 246 - Friday, December 21, 2012
    1. 77 FR 75784 - Disposal of Controlled Substances
      GPO FDSys XML | Text
      DEPARTMENT OF JUSTICE, Drug Enforcement Administration
      Notice of proposed rulemaking.
      Electronic comments must be submitted and written comments must be postmarked on or before February 19, 2013. Commenters should be aware that the electronic Federal Docket Management System will not accept comments after midnight Eastern Time on the last day of the comment period.
      21 CFR Parts 1300, 1301, 1304, 1305, 1307, 1317, and 1321