Local view for "http://purl.org/linkedpolitics/eu/plenary/2011-02-16-Speech-3-235-000"

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"en.20110216.11.3-235-000"2
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". To be able to better safeguard the distribution network for medicinal products it is crucial to have clear definitions not only of the scope, but also of the different actors in the supply chain. What is a falsified medicinal product? What is an active ingredient or an excipient? The Commission proposal does not provide the required clarity. The same applies for the definitions of the different actors in the chain of supply, clarifying their roles and responsibilities. It is essential to make a distinction between those actors who are already formally recognized - and which role is considered liable - and those who are outside that category, although being relevant to the liability of the distribution chain. Therefore it is important to make the distinction between traders and brokers, as well as to clarify their roles and responsibilities. The same applies for other actors, such as transporters or parallel traders. The directive should prevent confusion and should not allow any room for 'grey' areas. It should clearly identify which actors are able to operate in this domain and under which conditions. Clearer definitions will result in simpler implementation."@en1
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