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How to act in dossier evaluation

Suchergebnis_FormatLeitlinien Suchergebnis_Erscheinungsjahr 2019 How to act in dossier evaluation

The purpose of this practical guide is to explain in simple terms your duties regarding the content of your registration dossier …

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How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2014 How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID

This practical guide aims to assist registrants of intermediates and the downstream users in assessing if the use of a substance …

mehr erfahren: How to assess whether a substance is used as an intermediate under strictly controlled conditions and how to report the information for the intermediate registration in IUCLID …

How to prepare and develop a Substance Identity Profile (SIP)

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2018 How to prepare and develop a Substance Identity Profile (SIP)

This document provides practical advice to registrants on how to develop and maintain Substance Identity Profiles (SIPs) and …

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How to prepare a downstream user chemical safety report

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2015 How to prepare a downstream user chemical safety report

This practical guide aims to assist downstream users to perform chemical safety assessments to fulfil their duties under Article …

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How to prepare toxicological summaries in IUCLID and how to derive DNELs

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2012 How to prepare toxicological summaries in IUCLID and how to derive DNELs

In order to demonstrate the safe use of substances, registrants need to fulfil the information requirements as stipulated in …

mehr erfahren: How to prepare toxicological summaries in IUCLID and how to derive DNELs …

How to report robust study summaries

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2012 How to report robust study summaries

The purpose of this practical guide is to assist registrants in preparing the Robust Study Summaries for all endpoints that need …

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How to undertake a qualitative human health assessment and document it in a chemical safety report

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2012 How to undertake a qualitative human health assessment and document it in a chemical safety report

This practical guide aims to assist registrants to comply with their obligations in relation to the assessment of exposure and …

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Practical guide How to use and report (Q)SARs

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2016 Practical guide: How to use and report (Q)SARs

REACH foresees in Annex XI that the standard testing regime can be adapted by the use of non-test methods, such as …

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Practical guide: How to use alternatives to animal testing to fulfil your information requirements for REACH registration

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2016 Practical guide: How to use alternatives to animal testing to fulfil your information requirements for REACH registration

The REACH Regulation1 requires new information on hazardous properties to be generated avoiding unnecessary animal testing where …

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Practical guide for SME managers and REACH coordinators. How to fulfil your information requirements at tonnages 1-10 and 10-100 tonnes per year

Suchergebnis_FormatLeitlinien (in Englisch) Suchergebnis_Erscheinungsjahr 2016 Practical guide for SME managers and REACH coordinators

This Practical Guide is intended for people responsible for gathering all information needed to compile a technical dossier for …

mehr erfahren: Practical guide for SME managers and REACH coordinators …

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