State Codes and Statutes

Statutes > West-virginia > 60a > 60a-8-3

§60A-8-3. Purpose.
The purpose of this article is to implement the federal prescription drug marketing act of one thousand nine hundred eighty-seven ("PDMA"), U.S. Pubic 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 licensed 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 administration (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.

State Codes and Statutes

Statutes > West-virginia > 60a > 60a-8-3

§60A-8-3. Purpose.
The purpose of this article is to implement the federal prescription drug marketing act of one thousand nine hundred eighty-seven ("PDMA"), U.S. Pubic 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 licensed 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 administration (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.


State Codes and Statutes

State Codes and Statutes

Statutes > West-virginia > 60a > 60a-8-3

§60A-8-3. Purpose.
The purpose of this article is to implement the federal prescription drug marketing act of one thousand nine hundred eighty-seven ("PDMA"), U.S. Pubic 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 licensed 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 administration (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.