| Autor: |
Olivera, María Eugenia, Uema, Sonia Andrea Naeko, Romañuk, Carolina Beatriz, Caffaratti, Mariana, Mastroianni, Patricia Carvalho, Varallo, Fabiana Rossi, Vazquez, Marta, Fagiolino, Pietro, Maldonado, Cecilia, Vega, Elena María, Galvan, Zully Vera, Maidanag, Mabel, Acostag, Patricia, Rivero, Roxana, Barros, Carolina, Fontana, Daniela |
| Předmět: |
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| Zdroj: |
Pharmaceuticals Policy & Law; 2014, Vol. 16 Issue 3/4, p289-312, 24p, 3 Charts |
| Abstrakt: |
Pharmacovigilance is responsible for monitoring the safety of medicines in normal clinical use and during clinical trials. Legal requirements for pharmacovigilance in some Latin American countries (Argentina, Brazil, Chile, Paraguay and Uruguay) were reviewed. Disparities in the legal framework among the countries are observed being those for marketing authorization holders one of the most evident. The active rol of the universities and drug information centers for/of pharmacovilance seems to be a positive common point. Legal requirements regarding pharmacovigilance of biosimilar medicines, is still a point to be developed. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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