1. EC Council Directive 65/65/EEC 'On the
approximation of provisions laid down by law, regulation or administrative action relating
to proprietary medicinal products.'
2. EC Council Directive 75/318/EEC 'On the
approximation of laws of Member States relating to analytical, pharmacotoxicological and
clinical standards and protocols in respect of the testing of proprietary medicinal
products.'
3. EC Council Directive 87/22/EEC 'On the
approximation of national measures relating to the placing on the market of
high-technology medicinal products, particularly those derived from
biotechnology.'