What Is Directive 2001/83/Ec - Web directive 2001/83/ec of the european parliament and of the council show full title. Web directive 2001/83/ec of the european parliament and of the council. Web directive 2001/83/ec of the european parliament and of the c. Web it amended directive 2001/83/ec. Regulation (eu) 2017/745 is a regulation of the european union on. (5) oj l 147, 9.6.1975, p. Directive 2001/83/ec of the european parliament and of the council of 6 november. Web directive 2001/83/ec of the european parliament and of the council of 6 november 2001 on the community code relating to medicinal products for human use On the community code relating to medicinal products for human use. This directive introduces harmonised european measures to fight medicine falsifications and ensure that medicines are safe and that the.
Web commission directive 1999/83/ec (oj l 243, 15.9.1999, p. Web directive 2001/83/ec of the european parliament and of the council. This directive introduces harmonised european measures to fight medicine falsifications and ensure that medicines are safe and that the. Web directive 2001/83/ec of the european parliament and of the council of 6 november 2001 on the community code relating to medicinal products for human use 28.11.2001 en official journal of the european. Web directive 2001/83/ec, regulation (ec) no 178/2002, and regulation (ec) no 1223/2009. Web in november 2001, european parliament and the council adopted directive 2001/83/ec on the community code relating to medicinal products for human use. Directive 2001/83/ec of the european parliament and of the council of 6 november 2001 on the community code relating to medicinal products for human use. Web directive 2001/83/ec of the european parliament and of the council show full title. (5) oj l 147, 9.6.1975, p. Directive as last amended by. Web directive 2001/83/ec of the european parliament and of the council of 6 november 2001 on the community code relating to medicinal products for human use legislation.gov.uk. Web it amended directive 2001/83/ec. Web the legal basis for the qualified person is defined in the directive 2001/83/ec of the european parliament and of the council of 6 november 2001 on the. Web a generic medicinal product authorised pursuant to this provision shall not be placed on the market until ten years have elapsed from the initial authorisation of the reference. Web directive 2001/83/ec of the european parliament and of the c. Regulation (eu) 2017/745 is a regulation of the european union on. Directive 2001/83/ec of the european parliament and of the council of 6 november. On the community code relating to medicinal products for human use.