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Regulation of Medicinal Products for Human Use in the European Union

There is a considerable body of legislation governing the regulation of human medicinal products in the European Union. This legislation has evolved over the last fifty years, and it continues to evolve. The legislation is supported where necessary by scientific guidelines, including guidelines concerning safety aspects of medicines. The evaluation of human medicines is conducted through expert committees and subsidiary groups which cover all aspects of quality, safety and efficacy. This chapter discusses the evaluation of human medicinal products and the processes that lead to them gaining access to the commercial market, as well as the processes in place to ensure that marketed products continue to be monitored once in use.

Publication details

Print publication date
26 Feb 2018
Copyright year
Print ISBN
ePub eISBN
From the book series:
Issues in Toxicology