The European Federation of Pharmaceutical Industries Associations hasurged Members of the European Parliament to support the draft European Directive on the legal protection of biotechnological inventions (see also page 11), which has its first reading in the European Parliament this week (July 16).
The draft Directive does not create new legislation, but seeks to harmonize existing European law in this area. A previous draft Directive was rejected by the parliament two years ago (Marketletter March 20, 1995), following MEPs' concerns over a perceived lack of ethical safeguards.
The new compromise draft agreed by the parliament's Legal Affairs Committee aims to deal with these concerns by prohibiting any patenting relating to: the mere discovery of elements of the human body; the human body in its various stages of development; procedures for human reproductive cloning; and patenting of human germ-line therapy. It would also require that, for transgenic animals to be patented, evidence must be provided to show that the benefit to human beings would outweigh suffering to the animals. The new draft would also establish a European Ethics Advisory Committee.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze