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- W1480759737 abstract "This chapter contains sections titled: Introduction Development of the marketing authorisation system Path to the current European Union marketing authorisation system Centralised procedure Mutual recognition procedure Collaboration beyond the scope of the European Union Failing trust, competition, and limited resources Why are there two European procedures? Major criticisms of the system: science or politics? Perspective of legislation and subordination of the European Medicines Evaluation Agency Secrecy and transparency Race for the title of fastest drug regulatory agency Is it getting better? Review 2001 and G10 Medicines Group Limitations of the value of the clinical data used in licensing Conclusion References" @default.
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- W1480759737 date "2004-08-01" @default.
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- W1480759737 title "Development of Marketing Authorisation Procedures for Pharmaceuticals" @default.
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- W1480759737 doi "https://doi.org/10.1002/9780470994719.ch2" @default.
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