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Good clinical practice regulations

Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. [Pg.12]

The rules governing clinical trials in the United Kingdom are now set out in the Medicines for Human Use (Clinical Trials) Regulations 2004, which implement Directive 2001/20/EC on good clinical practice in the conduct of clinical trials. [Pg.387]

Non-clinical laboratory studies Good laboratory practice regulations, Fedl. Reg., (1978) 43, 59986. [Pg.148]


See other pages where Good clinical practice regulations is mentioned: [Pg.771]    [Pg.494]    [Pg.448]    [Pg.771]    [Pg.494]    [Pg.448]    [Pg.95]    [Pg.188]    [Pg.94]    [Pg.119]    [Pg.243]    [Pg.17]    [Pg.771]    [Pg.775]    [Pg.441]    [Pg.4]    [Pg.239]    [Pg.500]    [Pg.626]    [Pg.677]    [Pg.828]    [Pg.180]    [Pg.30]    [Pg.150]    [Pg.36]    [Pg.382]    [Pg.270]    [Pg.48]    [Pg.507]    [Pg.66]    [Pg.494]    [Pg.566]    [Pg.20]    [Pg.8]    [Pg.13]    [Pg.839]    [Pg.271]    [Pg.284]    [Pg.312]    [Pg.325]    [Pg.326]    [Pg.8]    [Pg.22]   
See also in sourсe #XX -- [ Pg.1783 , Pg.1925 , Pg.2486 , Pg.3064 ]




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