Examples of using The principles and guidelines in English and their translations into Slovenian
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Programming
It sets out the principles and guidelines of good manufacturing practice for medicines for animal use.
Commission Directive 2003/94/EC, of 8 October 2003, laying down the principles and guidelines of good manufacturing practice in.
(f) to comply with the principles and guidelines for good manufacturing practice for medicinal products as laid down by Community law.
However, we expect it to be possible to reach agreement on the principles and guidelines for further consideration of this package.
The principles and guidelines of good manufacturing practices for medicinal products referred to in Article 46(f) shall be adopted in the form of a directive.
We are distinguished by accuracy, precision and performance in accordance with the principles and guidelines of good laboratory practice.
(g) they must comply with the principles and guidelines of good distribution practice for medicinal products as laid down in Article 84.
Dried hemp is stored in premises specially designed for this purpose and in accordance with the principles and guidelines of good manufacturing practice.
It sets out the principles and guidelines of good manufacturing practice for medicinesand investigational medicines* for human use.
(2) Those principles and guidelines are set out in Commission Directive91/356/EEC of 13 June 1991 laying down the principles and guidelines of good manufacturing practice for medicinal products for human use(3).
The principles and guidelines of good manufacturing practices for medicinal products referred to in Article 46(f) shall be adopted in the form of a directive.
By means of the repeated inspections referred to in Article 26 of Directive 75/319/EEC,the Member States shall ensure that manufacturers respect the principles and guidelines of good manufacturing practice laid down by this Directive.
Laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use.
(1) All medicinal products for human use manufactured or imported into the Community, including medicinal products intended for export,are to be manufactured in accordance with the principles and guidelines of good manufacturing practice.
Laying down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use and investigational medicinal products for human use.
All medicinal products for human use manufactured or imported into Malta and the EU, including medicinal products intended for export,are to be manufactured in accordance with the principles and guidelines of Good Manufacturing Practice(GMP).
The principles and guidelines of good manufacturing practices for medicinal products referred to in Article 46(f) shall be adopted in the form of a directive, in accordance with the procedure referred to in Article 121(2).
In 2012,international partners will be engaged to make the principles and guidelines a shared framework for international collective engagement on long-term Internet resilience and stability.
The principles and guidelines of good manufacturing practice for veterinary medicinal products referred to in Article 50(f) shall be adopted by the Commission in the form of a Directive addressed to the Member States.
Ensures a quality system that rationally considers the principles and guidelines of good distribution practice for medicinal products with regard to traceability, transport and delivery of medicinal products to the delivery site;
This Directive lays down the principles and guidelines of good manufacturing practice for medicinal products for human use whose manufacture requires the authorization referred to in Article 16 of Directive 75/319/EEC.
They will accordingly observe the principles and guidelines deriving from those declarations, resolutions or other positions and will take such measures as may be necessary to ensure their implementation.
Croatia will accordingly observe the principles and guidelines deriving from those declarations, resolutions or other positions and will take such measures as may be necessary to ensure their implementation.
This includes compliance with the principles and guidelines of good manufacturing practices for medicinal products and the use of active substances that have been manufactured in accordance with good manufacturing practices for active substances and distributed in accordance with good distribution practices for active substances.