Framework for Implementation of Equivalence Requirements for Pharmaceutical Products
Abstract
This document has been prepared by the Working Group on BE (WG/BE) of the Pan American Network
on Drug Regulatory Harmonization (PANDRH) with the objectives of contributing to Drug Regulatory
Authorities (DRAs) of the Region of the Americas and recommending harmonized criteria concerning the
equivalence of drugs.
Subject
Collections
Related items
Showing items related by title, author, creator and subject.
-
Good manufacturing practices for pharmaceutical products: supplementary guidelines for the manufacture of investigational pharmaceutical products for studies in humans
Pan American Health Organization (1994) -
Transferring the financial risks of pharmaceutical benefits from a large health care provider in Argentina to a consortium of pharmaceutical companies
Cervellino, Juan C; Corazza, Sandra B; Bignone, Inés M. I; Fligman, M. Diana; Figueroa, Silvana; Roldán, Rubén; Morici, Pablo; Diez, Roberto A (2003) -
From medicinal plants to natural pharmaceuticals: the commercialization of nature
Pan American Health Organization; Souza Silva, José de (1996)III. Politics and policies