Good Laboratory Practicies - Product - specific legal acts

Good Laboratory Practicies - Product - specific legal acts

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

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Fonte: EU

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	Descrizione	Lingua	Dimensioni	Downloads
	Good Laboratory Practicies - Product - specific legal acts EU July 2022 Abbonati Chemicals	EN	289 kB	1