Examples of using The principles and guidelines in English and their translations into Swedish
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
including medicinal products intended for export should be manufactured in accordance with the principles and guidelines of good manufacturing practice;
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.
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.
The principles and guidelines of good manufacturing practice for veterinary medicinal products referred to in Article 50(f) shall be adopted in the form of a Directive addressed to the Member States in accordance with the procedure referred to in Article 892.
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 1212.
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.
Launching national, regional and local campaigns on the importance of interventions to reduce the unnecessary use of antimicrobial agents, and the principles and guidelines on good practice to motivate patients' adherence;
Partner organisations shall demonstrate in their application to be a KIC an agreement between themselves on the following issues in accordance with the principles and guidelines referred to in paragraph 1.
For the interpretation of the principles and guidelines of good manufacturing practice,and for investigational medicinal products.">
This Directive lays down the principles and guidelines of good manufacturing practice in respect of medicinal products for human use whose manufacture requires the authorisation referred to in Article 40 of Directive 2001/83/EC
The principles and guidelines are relevant to the involvement of expertise at all stages in the policymaking cycle,
The principles and guidelines thus cover the collection of advice though ad hoc