AgrotecHemp Corp.

6 Cited authorities

  1. Section 1051 - Application for registration; verification

    15 U.S.C. § 1051   Cited 3,923 times   127 Legal Analyses
    Requiring a filing of a Statement of Use to register a mark
  2. Section 355 - New drugs

    21 U.S.C. § 355   Cited 2,308 times   367 Legal Analyses
    Granting the court discretion to change the date on which an ANDA may be approved if "either party to the action failed to reasonably cooperate in expediting the action"
  3. Section 331 - Prohibited acts

    21 U.S.C. § 331   Cited 1,550 times   113 Legal Analyses
    Prohibiting "[t]he introduction or delivery for introduction into interstate commerce of any... drug ... that is adulterated or misbranded
  4. Section 321 - Definitions; generally

    21 U.S.C. § 321   Cited 1,186 times   179 Legal Analyses
    Defining “new drug”
  5. Section 262 - Regulation of biological products

    42 U.S.C. § 262   Cited 204 times   410 Legal Analyses
    Providing that a license shall issue "only upon a showing" by the manufacturer
  6. Section 357 - Qualification of drug development tools

    21 U.S.C. § 357   Cited 39 times   2 Legal Analyses

    (a) Process for qualification (1) In general The Secretary shall establish a process for the qualification of drug development tools for a proposed context of use under which- (A) (i) a requestor initiates such process by submitting a letter of intent to the Secretary; and (ii) the Secretary accepts or declines to accept such letter of intent; (B) (i) if the Secretary accepts the letter of intent, a requestor submits a qualification plan to the Secretary; and (ii) the Secretary accepts or declines