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European Agency for the Evaluation

CPMP Note for Guidance on the Investigation of Bioavailability and bioequivalence (CPMP/EWP/QWP/ 1401/98) The European Agency for the Evaluation of Medicinal Products, 2001. [Pg.527]

EMEA, European Agency for the Evaluation of Medical Products. Guideline on environmental impact assessment (EIAS) for veterinary medical products-phase I. CVMP/VICH/592/98-Final London 2000... [Pg.424]

European Union (EU). The European Agency for the Evaluation of Medical Products (EMEA) established January 2002 as the deadline for all electronically filed single case reports to be coded in MedDRA. All ADR drug reporting must be coded in MedDRA by January 2003. [Pg.853]

Includes information on the European Agency for the Evaluation of Medicinal Products. [Pg.982]

The European Agency for the Evaluation of Medicinal Prodncts, 2003. Note for guidance. AvaUahle http //enropa. en/agencies/community agencies/emea/index en.htm accessed 30 November 2009. [Pg.488]

See other pages where European Agency for the Evaluation is mentioned: [Pg.300]    [Pg.220]    [Pg.97]    [Pg.182]    [Pg.338]    [Pg.982]    [Pg.7]    [Pg.327]    [Pg.201]    [Pg.222]    [Pg.475]    [Pg.436]    [Pg.63]   


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European Agency for Evaluation

European Agency for the Evaluation Medicinal Products

European Agency for the Evaluation of Medicinal

European Agency for the Evaluation of Medicinal Products

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