Informazione tecnica HSE / 25 ° anno
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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
ECHA/PR/19/14
18 substances of very high concern (SVHCs) are recommended to be added to the REACH Authori...
Regolamento delegato (UE) 2019/1823 della Commissione dell’8 agosto 2019 che modifica il regolamento (UE) n. 528/2012 del Parlamento europeo e del Consiglio al fine ...
della Commissione del 3 febbraio 2021 recante modifica, ai fini dell’adeguamento al progresso tecnico e scientifico, dell’...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024