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United drug producer registration

Thus far, 37 guidelines aimed at both traditional and biotechnology-based products have been produced and are being implemented (Table 5). One of the ICHs most ambitious initiatives to date has been the development of the common technical document. This provides a harmonized format and content for new product authorization applications within the European Union, the United States, and Japan. When this and the other guidelines are fully implemented, considerable streamlining of the drug development and, in particular, registration process will be evident. This... [Pg.210]


See other pages where United drug producer registration is mentioned: [Pg.365]    [Pg.301]    [Pg.17]    [Pg.256]    [Pg.350]    [Pg.299]    [Pg.39]    [Pg.158]    [Pg.294]   
See also in sourсe #XX -- [ Pg.241 ]




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