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World Health Organization drug regulation

Source European Union (EU), US Food Drug Administration (FDA), and JECFA World Health Organization (WHO) regulations. ... [Pg.604]

World Health Organization. Effective drug regulation what can countries do ... [Pg.138]

Ratanwijitrasin S, Wondemagegnehu E. Effective drug regulation. A multicountry study. Geneva World Health Organization 2002. [Pg.77]

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]

The World Health Organization (WHO) issued the Ethical Criteria for Medicinal Drug Promotion in the late 1980s, which set out suggested standards to be implemented via regulation, international and national codes of practice. [Pg.18]

The conditions of production of pharmaceuticals are regulated by Good Practices in the Manufacture and Quality Control of Drugs (World Health Organization, No 226,1975, Annex 12.) and the Basic Standards and other guidelines of the Pharmaceutical Inspection Convention published by the Hungarian National institute of Pharmacy in Hungarian translation. [Pg.412]

See other pages where World Health Organization drug regulation is mentioned: [Pg.483]    [Pg.187]    [Pg.220]    [Pg.236]    [Pg.228]    [Pg.522]    [Pg.550]    [Pg.221]    [Pg.1211]    [Pg.120]    [Pg.561]    [Pg.355]    [Pg.37]    [Pg.243]    [Pg.2708]    [Pg.649]    [Pg.3749]    [Pg.272]    [Pg.231]    [Pg.218]    [Pg.315]    [Pg.164]    [Pg.1389]    [Pg.1115]    [Pg.113]    [Pg.347]    [Pg.438]    [Pg.205]    [Pg.397]    [Pg.443]    [Pg.2076]    [Pg.2077]    [Pg.3623]    [Pg.3624]    [Pg.323]    [Pg.249]    [Pg.425]    [Pg.35]    [Pg.174]    [Pg.2903]    [Pg.458]    [Pg.17]    [Pg.204]    [Pg.1955]   
See also in sourсe #XX -- [ Pg.65 ]



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