Übersetzung für "Gute herstellungspraxis" in Englisch

Validation studies should reinforce Good Manufacturing Practice and be conducted in accordance with defined procedures.

Good Manufacturing Practice Is concerned with both production and quality control.

The abbreviation GMP stands for Good Manufacturing Practice (good manufacture practice).

The contract shall clearly define the responsibilities of the contract manufacturer with regards to good manufacturing practice.

For the manufacturer to be able to comply with good manufacturing practice for investigational medicinal products, cooperation between the manufacturer and the sponsor is necessary.

These maximum levels must be safe and as low as reasonably achievable based upon good manufacturing practices.

Competent authorities shall enter the certificates of good manufacturing practice into the database for manufacturing authorisations.

Quality assurance: Maca Spirit is produced strictly following GMP guidelines (Good Manufacturing Practices).

Good manufacturing, technical and services jobs are being shipped to India, Asia, and other developing countries.

I believe it is also most important, so that we really can support homeopathic medicinal products, to have good manufacturing and laboratory practice and to make it possible to choose fantasy names.

Commission Regulation (EC) No 2023/2006 of 22 December 2006 on good manufacturing practice for materials and articles intended to come into contact with food is to be incorporated into the Agreement.

The provisions of this Sectoral Chapter cover all medicinal products which are industrially manufactured in Switzerland or the European Community, and to which Good Manufacturing Practice (GMP) requirements apply.

Labelling of investigational medicinal products intended for trials of that nature may be subject to simplified provisions laid down in the good manufacturing practice guidelines on investigational medicinal products.

I have also taken careful note of the interventions with regard to good manufacturing practice for food supplements, which is the subject of Amendment No 2.

These inspections were carried out by the Good Manufacturing Practice (GMP) Inspectorates of Belgium, Denmark, Germany, Spain, France, Ireland, Italy, the Netherlands, Portugal, Sweden, and the United Kingdom.

This will consist mainly of Good Manufacturing Practice (GMP) inspections to which will be added a number of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) inspections.

Equivalence between Member States' inspectorates is ensured and maintained in a variety of ways, including common legislation, common good manufacturing practice (GMP), common procedures for inspectorates, technical support, meetings, trainings, and internal and external audits.

In order to be imported into the EU, an active pharmaceutical ingredient needs to be accompanied by a Written Confirmation issued by the competent authority of the country where it is produced, confirming that the good manufacturing practice (GMP) applied is at least equivalent to the recognised EU GMP standards.