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
Regolamento (UE) 2017/542 della Commissione del 22 marzo 2017 che modifica il regolamento (CE) n. 1272/2008 (CLP) del Parlam...
Decreto 15 Febbraio 2019
Entrata in vigore dei testi, nelle lingue inglese e francese, pubblicati nel Supplemento 9.6 della Farmacopea eur...
della Commissione del 5 luglio 2021 che modifica gli allegati II e III del regolamento (CE) n. 1223/2009 del Parlamento europeo e del Consiglio sui prodotti cosmetici
GU L 23...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024
