ID 17095 | 14.07.2022
Good laboratory practice (GLP) is a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, archived and reported. Its purpose is to ensure the quality and integrity of the safety data submitted to regulatory authorities ('GLP receiving authorities').
The principles of GLP are applied to the non-clinical safety testing of test items contained in a range of products. The application of GLP is required by a variety of different product-specific legislation. This document lists all the EU legislation containing GLP provisions.
This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents. Only European Union legislation printed in the paper edition of the Official Journal of the European Union is deemed authentic.
1. Introduction
2. Chemicals
3. Biocides & pesticides
4. Food & feedstuff
5. Medicinal products
6. Cosmetics
7. Detergents
...
Fonte: EU
Collegati
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Abbonati Chemicals
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ID 21873 | 17.05.2024
Regolamento (UE) 2024/1328 della Commissione, del 16 maggio 2024, che modifica l’allegato XVII del r...
Decisione di esecuzione (UE) 2020/2182 della Commissione del 18 dicembre 2020 che stabilisce, a nome dell’Unione, la risposta definitiva sulla futura importazione...
November 2021
Executive summary
1. Introduction
2. Summary of the Authorisation process
2.1. Can...
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