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
Ministero della Salute 03 Ottobre 2017
Documento di orientamento prodotti ...
REACH Authorisation Decisions List of authorisation decisions adopted on the basis of Article 64 of Regulation (EC) No 1907/2006 (REACH). The list also includes refer...
Helsinki 08.08.2017
Subject: Global 2000’s report on glyphosate
Further to our initial response (published on ECHA’s website on 13 July 2017), ECHA ...
Testata editoriale iscritta al n. 22/2024 del registro periodici della cancelleria del Tribunale di Perugia in data 19.11.2024
