National Medication, Food and Medical Technology Administration (ANMAT) - Entity in charge of authorization procedures, registration, regulation and supervision of pharmaceutical products in Argentina.
National Institute of Food and Drug Monitoring (Invima) - governmental body that exercises the functions of inspection and surveillance of pharmaceutical industries in Colombia.
General Directorate of Medicines, Supplies and Drugs (Digemid) - Technical ORGAO do Ministério da Saúde pela responsável fiscalização of drug qualidade not Peru.
Prequalification of the Pan American Health Organization (PAHO) - Brazilian pharmaceutical Single integrate PAHO suppliers group, linked to the United Nations (UN).
Certificate of Good Practices on Bioequivalence (Anvisa) - The Magabi Clinical Researches represents the country in the Global Bioanalysis Consortium.
Brazilian Network of Health Analytical Laboratories (Reblas) - official Entity authorized by Anvisa to perform pharmaceutical equivalence tests.
Good Manufacturing Practices (GMP) – In all industrial segments in which it operates, Eurofarma also maintains strict compliance with the standards of Good Manufacturing Practices (GMP), based on regulations in force in the country, established and supervised by Anvisa.