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Regulatory authorities World Health Organization

One of the many challenges facing regulatory authorities worldwide is that of counterfeit drugs. The World Health Organization (WHO) defined... [Pg.269]

WHO. A legislative scheme for regulating medicinal products for adaptation by small national drug regulatory authorities with limited manpower and other resources. Geneva World Health Organization 1993. (WHO/PHARM/93.244 annex 3). [Pg.77]

WHO. Marketing authorization of pharmaceutical products with special reference to multisource (generic) products. A manual for a drug regulatory authority. Geneva World Health Organization 1999. (WHO/DMP/RGS/98.5). [Pg.77]

See other pages where Regulatory authorities World Health Organization is mentioned: [Pg.333]    [Pg.1083]    [Pg.342]    [Pg.844]    [Pg.66]    [Pg.544]    [Pg.220]    [Pg.499]    [Pg.115]    [Pg.2786]    [Pg.190]    [Pg.140]    [Pg.231]    [Pg.536]    [Pg.736]    [Pg.269]    [Pg.916]    [Pg.1389]    [Pg.69]    [Pg.347]    [Pg.380]    [Pg.383]    [Pg.1018]    [Pg.47]    [Pg.307]    [Pg.17]    [Pg.70]    [Pg.35]    [Pg.131]   
See also in sourсe #XX -- [ Pg.222 , Pg.227 ]



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Health authorities

Regulatory authorities

World Health

World Health Organization

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