Page 124 - 71_01
P. 124
ANA I. TORRES SUÁREZ Y M.a ESTHER GIL ALEGRE AN. R. ACAD. NAC. FARM.
(3) WHO (1996). «Stability Testing of Pharmaceutical Products Containing Well
Established Drug Substances in Conventional Dosage Forms». WHO Technical
Report Series, n.º 863, Annex 5.
(4) WHO (2001). Report of the thirty seventh meeting of the WHO Expert Com-
mittee on Specifications for Pharmaceutical Preparations (October 2001) Gi-
nebra, págs. 22-26.
(5) GRIMM, W. (1993). «Storage Conditions For The Most Important Market For
Drug Products, Including The EU, Japan And The USA». Drug Dev. Ind.
Pharm., 19, págs. 2795-2830.
(6) BRAHMAIAH, K. & RHODES, C. T. (1999). «Trends In Stability Testing, With
Emphasis On Stability During Distribution And Storage». Drug Dev. Ind.
Pharm., 25(7), págs. 857-868.
(7) INSTITUTO NACIONAL DE METEOROLOGÍA (1991). Guía Resumida del Clima en Espa-
ña, 1961-1990. Centro de Publicaciones del Ministerio de Medio Ambiente.
Madrid.
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