The purpose of this article is to protect the health, safety and general welfare of residents of
this state and to implement the federal Prescription Drug Marketing Act of 1987 ("PDMA"),
U. S. Public Law 100-293, 102 Stat. 95, codified at 21 U. S. Code §321; and particularly
PDMA requirements that no person or entity may engage in the wholesale distribution of
human prescription drugs in any state unless such person or entity is licenseed by such state
in accordance with federally-prescribed minimum standards, terms and conditions as set
forth in guidelines issued by United States food and drug administratiorn (FDA) regulations
pursuant to 21 U. S. Code §353(e)(2)(A) and (B); and such regulations as are set forth in 21
C. F. R. Part 205.‹ Prev All West Virginia sections Next ›
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