Skip to main content Skip to office menu Skip to footer
Capital IconMinnesota Legislature

Office of the Revisor of Statutes


A person engaged in the manufacturing of drugs, medicines, chemicals, or poisons for medicinal purposes whose place of business is located in Minnesota must comply with the current Good Manufacturing Practices regulations for finished pharmaceuticals published by the United States Food and Drug Administration.

Statutory Authority:

MS s 151.06


18 SR 1145

Published Electronically:

September 21, 2011

Official Publication of the State of Minnesota
Revisor of Statutes