PDMA definition

PDMA means the Prescription Drug Marketing Act of 1987, as amended, and the regulations promulgated thereunder from time to time.

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PDMA means the Prescription Drug Marketing Act.

PDMA means Provincial Disaster Management Authority, Punjab

Examples of PDMA in a sentence

• Words have their normal meaning under the language of this PDMA unless specifically defined.

• Interpreting the conditions in this PDMA, singular also means plural, male also means female or neuter, and the other way around.

• ICS will adhere to its standard operating procedures for distribution of Sample Products to Recipients, as well as all Requirements of Law, including without limitation the PDMA, pertaining to distribution of samples to Recipients.

• The Company and ICS will create and maintain all applicable forms and records required by all Requirements of Law applicable to warehousing and distribution of Samples and Free Goods including PDMA, Rules and Controlled Substance Laws.

• To receive credit, a signed and dated PDMA return certification must accompany all prescription drug returns.

More Definitions of PDMA

PDMA means the Prescription Drug Marketing Act of 1987, 21 U.S.C. §§ 321 et seq. (or any successor thereto), as amended from time to time, and the rules, regulations, guidelines, guidance documents and compliance policy guides issued or promulgated thereunder.

PDMA means the Prescription Drug Marketing Act of 1987, as amended, and the rules, regulations and guidelines promulgated thereunder and in effect from time to time, and any foreign counterpart thereto.

PDMA shall have the meaning ascribed in Article 4.14 hereof.

PDMA means Professional Data Management Again, Inc.

PDMA means the Prescription Drug Marketing Act, Public Law No. 100-293, 102 Stat. 95 (Apr. 22, 1988), as subsequently amended and codified.

PDMA means the Prescription Drug Marketing Act, and relevant regulations and guidelines promulgated thereunder.

PDMA means the Prescription Drug Marketing Act of 1987. The PDMA establishes legal safeguards for prescription drug distribution to ensure safe and effective pharmaceuticals and is designed to discourage the sale of counterfeit, adulterated, misbranded, subpotent, and expired prescription drugs.