Local view for "http://purl.org/linkedpolitics/eu/plenary/2008-10-22-Speech-3-025"

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"en.20081022.2.3-025"2
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"Mr President, I would like to take the liberty of giving a general, overall perspective since, up to now, EU harmonisation of medicinal product legislation has only involved relaxing the rules in Denmark. and the sale of medicines has increased. The new proposal with regard to marketing authorisations for medicines extends a helping hand to the pharmaceuticals industry. It will, in general, be easier to make small changes to medicines and release them under the same name, as mentioned by the previous speaker and, at the same time, it will be easier to change the name of a product if it is to be sold to treat a different pathology. There is a fear that these changes could make it more difficult for consumers to see the wood for the trees and make life easier for the pharmaceuticals industry. We also need to give consideration to the fact that the relationship between easier access to the authorisation of medicines and an increased risk for consumers is often, unfortunately, directly proportional. I am not saying that we should put unnecessary administrative obstacles in the way of the industry, but neither should we accept a slackening of the reins to make it easier for the pharmaceuticals industry to make a profit when it is people’s health and the health of animals that are at stake. In doing this, we will purely and simply be barking up the wrong tree. If we view it in a wider context, this directive is part of the industry’s efforts to improve profits in relation to the US. Let us not be naïve. We must not allow ourselves to be misled by fine-sounding, but empty statements relating to patients and consumers."@en1
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