The Rules Governing Medicinal Products in the European Community: v. 1

The regulatory provisions relating to medicinal products for human use are presented in this report, fully revised in September 1991. It outlines EC directives relating to the marketing authorization for medicinal products for human use and the pricing of medicinal products for human use. The book may be of use to those involved in the production and use of medicinal products within the European Community.
 
The regulatory provisions relating to medicinal products for human use are presented in this report, fully revised in September 1991. It outlines EC directives relating to the marketing authorization for medicinal products for human use and the pricing of medicinal products for human use. The book may be of use to those involved in the production and use of medicinal products within the European Community.