Примери за използване на Falsified medicinal на Английски и техните преводи на Български
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One of the reasons for this is that falsified medicinal products and drugs sold in places not authorised to sell them do not meet the quality requirements set for medicinal products,
The purpose of the regulation is to prevent entry into the legal supply chain of falsified medicinal products and to ensure product integrity and authentication of medicines(ie. safety features
in recent years the number of falsified medicinal products has increased exponentially,
The majority of requirements of the new legislation that will help to prevent entry into the legal supply chain of falsified medicinal products will come into force in January 2013, but preparatory work has to be undertaken in 2012.
the shadow rapporteurs for their excellent work on an important matter, because falsified medicinal products clearly represent a serious threat to patients' health.
I believe the implementation of new rules is key to protecting patients from falsified medicinal products.
WHO estimates indicate that falsified medicinal products are circulated in large quantities in EU Member States.
The introduction of a system for the verification of medicinal products throughout Europe is a key measure to ensure patient safety by preventing the entry of falsified medicinal products into the legal supply chain.
not to mention the fact that falsified medicinal products may contain sub-standard active ingredients.
as well as on online sales, are further measures that I think will curb the trade in falsified medicinal products.
I think it is a good text which protects patients from the great dangers arising from taking falsified medicinal products.
because this is one of the main routes for falsified medicinal products to enter the European market.
I voted for the report by Mrs Matias since the entry of falsified medicinal products into the legal supply chain poses a threat to the entire European pharmaceutical system,
to prevent the entry of falsified medicinal products, thus achieving a positive
In particular, I would stress that the Commission's proposal fails to provide exhaustive answers concerning the nature and characteristics of a falsified medicinal product, active ingredient
(1) Directive 2001/83/EC, as amended, provides for measures to prevent the entry into the legal supply chain of falsified medicinal products by requiring the placing of safety features consisting of a unique identifier
In writing.-(RO) Falsified medicinal products pose a real threat to the entire pharmaceutical system in Europe since,
unambiguous definition of a'falsified medicinal product'. but also to define all the entities in the distribution chain,
although the Commission's proposed changes to the directive on medicinal products for human use are designed to help prevent the entry of falsified medicinal products, we would have expected more concrete results,
I fully support the proposal that measures should be taken with the aim of minimising the problem of trade in falsified medicinal products, and also of trade in medicines sold in places not authorised to sell them