Local view for "http://purl.org/linkedpolitics/eu/plenary/2007-03-29-Speech-4-106"

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"en.20070329.23.4-106"2
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". I have voted in favour of the report by my colleague Mr Ulmer on the amendment of various directives on medical products. The term ‘medical products’ covers a wide range of products including syringes, spectacles, diagnostic equipment, small devices capable of being implanted, medical imaging technology, etc., and it became a matter of absolute necessity to enhance competitiveness and medical safety in this sector. In order to do this, the present legislative framework, consisting of three directives which define the basic requirements to which medical equipment must conform, needed to be improved, particularly as regards, inter alia, clinical evaluation, transparency, the monitoring of markets, custom-made devices, the use of human tissue and coordination between independent bodies. The practical provisions that we have adopted in this document will improve the harmonisation of this highly complex and diverse sector by making the rules applicable to it clearer and simpler. It is worthy of note that many industrial companies in this sector operate on the global market and so it is necessary that efforts be made to encourage the process of international cooperation, especially through the harmonisation of standards."@en1

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