Básica:
Sites de Agências Regulatórias ANVISA (Brasil), EMEA (Europa) e FDA (USA): Ensaios Clínicos e Registros de novos
medicamentos .
CATO, A.E.; SUTTON, L.; CATO, A. Clinical drug trials and tribulations (drugs and the pharmaceutical sciences, vol 120). 2nd ed. New York: Marcel Dekker, 2002.
KIMKO, H.C.; DUFFULL, S.B. Simulation for designing clinical trials: a pharmacokinetic-pharmacodynamic modeling perspective (drugs and the pharmaceutical sciences, vol 127). New York: Marcel Dekker, 2003.
LEE, A.. Adverse Drug Effects. 2nd ed. Royal Pharmaceutical Society Great Britain/RPS Publishing, London, 2006.
LIPSCOMB JC OHANIAN, EV.. Toxicokinetics and Risk Assessment. Informa Healthcare USA, Inc., 2007.
Complementar:
BRUNTON, LL.; CHABNER, BA.; KNOLLMANN, BC. (ed). Goodman & Gilman's The pharmacological basis of therapeutics. 12 th ed. New York: McGraw-Hill, 2012.
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