EU pharmaceuticals news in brief

Published: 13-Aug-2009

The European Medicines Agency (EMEA) has released proposed changes to Guidelines on product information for human vaccines.


The European Medicines Agency (EMEA) has released proposed changes to Guidelines on product information for human vaccines.

The agency has also released a Guideline on the required data for certifying of advanced medical therapy products.

It has published a paper on Guidelines for using transgenic animals to make biological medicinal products.

EMEA has also released papers on the Clinical investigation of medicines treating lipid disorders and hypertension.

Meanwhile, the European Commission has noted that a new Regulation on maximum residue limits of pharmacologically active substances in animal foods has come into force.

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