Estudio sobre las condiciones actuales de los Laboratorios Oficiales de Control de Calidad de Medicamentos (LOCM) en América Latina y el Caribe

This document, which permits to conduct a diagnostic study of the Medicine Control Laboratory, was prepared in PAHO/WHO by Jose M. Parisi being based on the WHO recommendations for Good Manufacture Practices (GMP) (32nd Report, 1992, and its updates).

The document was reviewed by the Working Group on Good Laboratory Practice (GLP/WG) within the framework of the Pan American Network for the Drug Regulatory Harmonization (PANDRH) during the Fifth Meeting, carried out in Guatemala City (28 May to 1 June 2007) and presented at the V PARF Conference, in November 2008.