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EudraLex - Volume 1 - Pharmaceutical legislation for medicinal products for human use | Public Health
2015 marks the 50th anniversary of pharmaceutical legislation in the EU, which began with the adoption of Directive 65/65 in 1965. Today the EU legal framework for medicinal products for human use guarantees high standards of quality and safety of medicinal products, while promoting the good functioning of the internal market with measures that encourage innovation and competiveness. Directives Regulations Non-Legislative acts Miscellaneous Directives Regulations Non-legislative acts Miscellaneous
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