Examples of using Centralised procedure in English and their translations into Dutch
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Medicine
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Official
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Colloquial
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Ecclesiastic
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Financial
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Computer
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Ecclesiastic
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Official/political
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Programming
It introduces flexibility to the system whilst still allowing the pharmaceutical industry to benefit more from the centralised procedure.
The EMA is responsible for the scientific evaluation of applications for European marketing authorisation for medicinal products centralised procedure.
animal use derived from biotechnology and other high-technology processes must be approved via the centralised procedure.
the timelines for these product-types to be eligible for the centralised procedure as proposed by the Council;
This centralised procedure has so far led to authorisations for 155 biotechnology or innovative medicines.
The adjustment of the timeline for the remaining centralised procedure should help accelerate the investigation phase of the procedure. .
The real impact of the reorganisation on the operation of the centralised procedure will only become fully apparent in 2002 once additional resources are available.
For medicinal products other than those that have to be authorised via the mandatory centralised procedure, an abridged application can be filed after eight years and no additional year may be obtained.
Withdrawal of applications in the centralised procedure is possible before the CPMP issues an opinion.
The proposal lays down a centralised procedure by which the Commission will authorise the placing on the market
The centralised procedure is compulsory for medicinal products derived from biotechnology,
The centralised procedure usually deals with highly innovative medicinal products,
One of the most criticised areas of the centralised procedure is the decision-making process that follows the scientific evaluation by the EMEA.
The centralised procedure via the EMEA in London is increasingly becoming the norm for an increasing number of medicinal products.
A credible application of the centralised procedure for marketing medicinal products cannot work without this sort of approach.
The broadening in scope of the centralised procedure will bring administrative savings for companies able to benefit from the single application procedure. .
The centralised procedure is mandatory for all veterinary medicinal products derived from biotechnology
The centralised procedure tends to be used predominantly by large multinational companies
The centralised procedure tends to be used predominately by large multi-national companies
Option B: Centralised procedure for evaluation of new AS with binding time limits.