Voorbeelden van het gebruik van Manufacturing practice in het Engels en hun vertalingen in het Nederlands
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Medicine
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Colloquial
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Official
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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
There must be evidence that the drug product is manufactured according to Good Manufacturing Practice GMP.
Inspectors prepared a Community Guide to Good Manufacturing Practice, which was used by the Commission as the basis for the drafting of the directive.
GMP stands for Good Manufacturing Practice and is a set of guidelines for assuring the quality of production processes.
guidelines for good manufacturing practice for medicinal products for human use.
Directive 91/356/EEC(OJ L 193, 17.7.1991) Good manufacturing practice for medicinal products for human use Germany.
Competent authorities shall enter the certificates of good manufacturing practice into the database for manufacturing authorisations.
In order to enforce good manufacturing practice and to protect the health of consumers,
The technique, if applied using good manufacturing practice, will not substitute for good hygiene practices. .
All these raw materials are manufactured in accordance with the strict GMP-standards(Good Manufacturing Practice).
The Committee considers the use of this compound acceptable as a solvent for the extraction of food provided the levels of residues comply with good manufacturing practice.
products for human use, the two others concerning good manufacturing practice.
The rules governing medicinal products in the European Community Volume IV- Good manufacturing practice for medicinal products.
The ISPE's guide The Good Automated Manufacturing Practice(GAMP) Guide for Validation of Automated Systems in Pharmaceutical Manufacture describes a set of principles and procedures that help
the guidelines on good manufacturing practice for medicinal products
Letter of Invitation to Good Manufacturing Practice(“GMP”) Inspection:
To manage the ad hoc Meetings of good manufacturing practice(GMP) and good clinical practice(GCP)
guidelines of good manufacturing practice for veterinary medicinal products whose manufacture requires the authorization referred to in Article 24 of Directive 81/851/EEC.
That's why the entire TPW™ Pack Deals range is packaged under strict Good Manufacturing Practice and made in sealable,
guidelines of good manufacturing practice and shall submit to inspections carried out by the competent authorities as provided for by Article 26 of Directive 75/319/EEC.
Volume IV contains a Community guide to Good Manufacturing Practice In the manufacture of medicinal products