Specific reports

ECHA reports focused on specific issues, as described below.


The reports in this section do not represent the official views or position of ECHA. Some of them summarise the discussions at workshops organised by ECHA on topical issues in regulatory science. The Agency may also commission work by consultants, such as survey projects or state-of-the-art reviews, and the reports here present their findings.


Title Description Date of publication  
Report on the potential scope and number of applications submitted to ECHA for the European Positive Lists This report presents the findings of a stakeholder engagement exercise undertaken by an external contractor to obtain feedback on the then draft European Positive Lists generated under Article 11 of the Drinking Water Directive. The exercise aimed to (a) understand the potential scope and interest amongst stakeholders regarding the number of future applications submitted to ECHA, (b) identify substances which may be omitted from the first European Positive Lists, and (c) identify stakeholders with an interest in joining ECHA user groups to support the development of the DWD application process. April 2024 Report
New Approach Methodologies Workshop: Towards an Animal-Free Regulatory System for Industrial Chemicals. This report presents the main findings from the European Chemicals Agency’s New Approach Methodologies (NAM) workshop “Towards an Animal-Free Regulatory System for Industrial Chemicals” (31 May – 1 June 2023). The aim of the workshop was to discuss how to support the transition to an animal-free regulatory system for chemical safety assessment and build a common understanding between stakeholders on what New Approach Methodologies (NAMs), can achieve in the short and long term. September 2023 Report
Key Areas of Regulatory Challenge ECHA has started to map key areas of regulatory challenge (KARC) under the umbrella of the PARC Project that provides a forum for collaboration across Europe and aims to pioneer scientific areas addressing most urgent regulatory challenges. The identified key areas of regulatory challenge are formulated as an ‘evolving research and development agenda’ aiming to support and inspire the scientific research community. The overview presented in this report is not an exclusive list and other areas of relevance are currently under development. This report will be updated and refined as the scientific areas evolve and key regulatory challenges develop. September 2023 Report
Final report of the Study on the Role of Robust Study Summaries (RSS) in Hazard Assessment (3/3) This third and final report of the RSS project highlights a series of recommendations to improve the RSS concept. This report is part of a project ECHA launched in 2021 together with the OECD, to improve the study summary formats. The first report on the initial feedback collected from stakeholders was published in April 2022. The second report analysed whether the RSS accurately summarise studies so that the hazards of tested substances could be properly assessed without accessing the full study report. April 2023 Report
Study on the Role of Robust Study Summaries in Hazard Assessment (2/3): Analysis of the accuracy of RSS This second report of the project to improve robust study summaries (RSS) analyses a series of RSSs. It gauges whether they accurately summarise studies so that the hazards of tested substances can be properly assessed without accessing the full study report. ECHA also publishes a Standard Operating Procedure with instructions for authors to write ideal RSSs from the full study reports. This report is part of a project ECHA launched in 2021 together with the OECD, to improve the study summary formats. The first report on the initial feedback collected from stakeholders was published in April 2022. The final report with the recommendations for improvements will be published later this year. March 2023 Report

Standard Operating Procedure
Evaluating results from 55 extended one-generation reproductive toxicity studies under REACH This report contains the key findings of evaluating 55 extended one-generation reproductive toxicity studies (EOGRTS). It gives recommendations how to improve the EOGRTS. March 2023 Final report
Bioaccumulation assessment of air-breathing mammals This discussion paper presents the scientific background and current knowledge on bioaccumulation in air-breathing organisms. It discusses a tiered assessment approach, and available methods. November 2022 Download
Sterile controls in biodegradation studies – current status in regulatory testing in persistence assessment under REACH This ECHA note presents the current status of the use of sterile controls in biodegradation studies. The note also includes a review of commonly used sterilisation methods and advice on the inclusion and implementation of sterile controls in degradation studies for persistence assessment.  November 2022 Download
Options to assess persistence of volatile substances in regulatory PBT assessment This ECHA note presents the options to assess persistence of volatile substances in PBT assessment. The note includes advice on the use of indicators for assessing the volatility of the substances, options to address volatile substances in simulation degradation studies and advice on data treatment and interpretation from these studies.  November 2022 Download
Changes of market volumes of chemicals subject to authorisation in 2010-21 This report presents estimates for changes in market volumes of substances that have been placed on the EU market that are subject to REACH authorisation from 2010 to 2021. The estimates are based on information from registration dossiers, from applications for authorisation and other sources.  October 2022 Download
European arthropods and their role in pollination: scientific report of their biodiversity, ecology and sensitivity to biocides This scientific report describes in detail the biodiversity and the ecology of the following four insect orders: Diptera, Lepidoptera, Coleoptera and Hymenoptera, that together cover the majority of flower visiting insects, focusing on the sensitivity of these organisms to biocidal products.  September 2022


Report [PDF]
Annex I [XLSX]
Annex II  [XLSX]
Annex III  [XLSX]
Annex IV [XLSX]
Annex V [XLSX]

Study on the Role of Robust Study Summaries in Hazard Assessment (1/3): Survey and interviews report In 2021, ECHA launched a project, in collaboration with the OECD, with the aim to identify improvements to the study summary formats developed at OECD level that will increase trust in the robust study summary (RSS) concept. This report wraps up the initial feedback collected from experienced authors, evaluators and other type of actors (NGOs, academia, etc.) making use of the study summaries in the context of chemical hazard assessment. The project will conclude in December 2022 with the recommendations for improvement and a final report will also be published. April 2022 Download
Case study: Impacts of REACH 
authorisation of trichloroethylene
This report takes a detailed look at the impacts of REACH authorisation on trichloroethylene (TCE) from its inclusion on the Candidate List in 2010 until January 2022. The need to obtain authorisation significantly reduced the use of TCE. The annual use of TCE in the EU has dropped more than 95 % in the past 12 years.   March 2022 Download
Chemical Recycling of Polymeric Materials from Waste in the Circular Economy The purpose of this study is to investigate the current state of knowledge regarding the chemical recycling of polymeric materials (e.g., plastics, rubber) from waste. Considering the scale of plastic pollution and the potential role that chemical recycling could play in addressing some of the related issues, this study focused on chemical recycling of plastic waste. November 2021 Download
Chemical Recycling of Polymeric Materials from Waste in the Circular Economy The purpose of this study is to investigate the current state of knowledge regarding the chemical recycling of polymeric materials (e.g., plastics, rubber) from waste. Considering the scale of plastic pollution and the potential role that chemical recycling could play in addressing some of the related issues, this study focused on chemical recycling of plastic waste. November 2021 Download
Causal impacts of the REACH Authorisation process on the use of substances of very high concern in the EU This report presents two case studies that seek to quantify the causal effects that regulatory actions under the REACH Authorisation title have had on the use of specific substances of very high concern (SVHCs) in the EU/EEA. November 2021 Download
Substitution of trichloroethylene in metal parts cleaning in the European Union The study investigates which solvents and methods have replaced trichloroethylene in the metal parts cleaning industry within the European Union. The study is based on an industry survey, distributed to former users of trichloroethylene in metal parts cleaning. The study indicates that the main substitute for trichloroethylene is the chemically similar substance: perchloroethylene. The study has been carried out by researchers at the FRAM centre, University of Gothenburg, Sweden. July 2021 Download
Costs and benefits of REACH restrictions proposed between 2016-2020 This report summarises and aggregates the benefits to human health and the environment as well as the costs associated with REACH restriction dossiers and the opinions of ECHA’s Committees for Risk Assessment (RAC) and Socio-economic Analysis (SEAC). February 2021 Download
Critical literature review of analytical methods applicable for environmental fate studies

The aim of the report, commissioned by ECHA, is to provide thorough, transparent and critical literature review of analytical methods (and their limitations) applicable for environmental fate studies (e.g. for OECD Test Guidelines (TG) 305, 307, 308 and 309). The data gathered were analysed in the context of the v(P)v(BT) assessment under the REACH and the Biocidal Products Regulations. The review also covered the methodologies applied under other EU regulatory regimes.

February 2021 Final report

Executive summary
Socio-economic impacts of REACH authorisations

This report is a meta-analysis of the state of play of applications for authorisation presenting ECHA’s analysis on socio-economic impacts based on the data and knowledge gathered while implementing the authorisation process.

January 2021 Download
The use of PFAS and fluorine-free alternatives in textiles, upholstery, carpets, leather and apparel This report is the outcome of a study contracted by the European Commission on the use of PFAS and fluorine-free alternatives in textiles, upholstery, carpets, leather and apparel. It has been prepared by Wood, Ramboll and PFA Brussels. December 2020 Download
Impacts of REACH restriction and authorisation on substitution in the EU This report provides the latest information on how authorisation promotes the substitution of substances of very high concern (SVHCs) with safer alternatives, but also includes the impact of restrictions under REACH as part of its scope, with the goal of understanding the impacts of both processes on the substitution of hazardous chemicals in the EU. July 2020 Download
The use of PFAS and fluorine-free alternatives in fire-fighting foams This report combines two studies on “The use of PFASs and fluorine-free alternatives in fire-fighting foams” (commissioned by the European Commission) and an “Assessment of alternatives to PFAS-containing fire-fighting foams and the socio-economic impacts of substitution” (commissioned by ECHA). It is prepared by Wood working in partnership with Ramboll and COWI. June 2020 Download
Use of bisphenol A and its alternatives in thermal paper in the EU The purpose of the report is to monitor the extent to which BPA is being replaced by BPS and other developers following the publication of Commission Regulation (EU) 2016/2235 concerning the restriction of BPA in thermal paper. The restriction applies as of 2 January 2020. The first report was published in 2017 and the last in 2020. December 2017 - June 2020

Download (2020)

Download (2019)

Download (2018)

Download (2017)

Report on non-extractable residues

The aim of the document, commissioned by ECHA, is to improve the interpretation of non-extractable residues in the persistence assessment of substances. The document reviews the state-of-science on their role in degradation assessment in soil, sediment and water with suspended solids. It will be used as background document for the persistence assessment of substances under REACH and the Biocidal Products Regulation.


Joint Report ECHA and UBA
Expert Workshop on the potential regulatory application of the Fish Embryo Acute Toxicity (FET) Test under REACH, CLP and the BPR

ECHA and the German Environment Agency UBA organised an expert workshop on the potential regulatory application on the FET test in May 2017. 

The report on the regulatory applicability of non-animal approaches reviews their current status under the EU chemicals legislation. It describes the main types of non-animal approaches, adaptation rules, information requirements and needs for relevant (eco)toxicological properties. For each relevant information requirement, the report describes the potential non-animal approaches, the challenges and future perspectives. November 2017 Download
Segmentation of potential SME Market for ECHA Cloud Services for REACH Registration This study on the segmentation of the small and medium-sized enterprise (SME) market confirms uncertainties regarding the SMEs’ intentions to register their substances by the 31 May 2018 deadline. The main hurdle seems to be the cost of data needed for registration. It also makes recommendations for the Agency on how to convince SMEs to use and benefit from the ECHA Cloud Services. October 2017 Download
Insights on the impact of REACH & CLP implementation on industry’s strategies in the context of sustainability Several large corporations (e.g. stock-listed companies) have for a number of years included focuses on sustainable development, Responsible Care and corporate social responsibility in their business activities. Sustainability is often mentioned as a key goal by organisations and many of them are actively integrating sustainability principles into their business models.

Today, social trends around sustainability as well as emerging regulatory requirements are seen to create both pressure and opportunities for companies. When it comes to compliance with chemical regulations, some companies see it only as a burden, whereas others try to turn the compliance obligations into business opportunities.
September 2017 Download
Socio-economic impacts of REACH authorisations One new element of the REACH Regulation is the authorisation title. It aims to ensure a sufficiently high level of protection for human health and the environment whilst allowing firms to continue the use of specific substances of very high concern (SVHCs), if the risks are adequately controlled. Otherwise, uses may still be authorised if the socio-economic benefits from the use of the substance are shown to outweigh the risks connected with its use and there are no suitable alternative substances or technologies that are economically and technically viable. Taking into account the good functioning of the internal market, the European Commission would grant an authorisation for the continued use. September 2017 Download
Scientific review on the link between the narcotic effects of solvents and (developmental) neurotoxicity. This scientific report summarises the current evidence on adverse neurological effects exerted by organic solvents with narcotic properties. Information on neurotoxicity in both adults and developing organisms are presented. It has been acknowledged that neurotoxicity in adult animals is a particular concern for developmental neurotoxicity. The question whether narcosis in adult animals should be considered as a concern for developmental neurotoxicity is addressed. June 2017 Download
Study on the effects of the process of applying for authoristation for chemicals on the athorisation list. 14 Finnish companies and a national competent authority were interviewed by Aalto University students to find out how the process of applying for authorisation to continue using  chemicals that are on the authorisation list of REACH affected them. The study, commissioned by ECHA, identified improved networking of companies who participated in consortiums, improved worker protection, accelerated substitution and increased awareness of the safety aspects of alternatives in some of the companies. The report highlights the importance of an effective flow of information between all relevant actors (applicants, suppliers, customers, consultants, sector associations and authorities). The report also gives an overview of the time and cost distribution companies had to invest in their applications. According to the report companies have not passed on the costs of applications for authorisation to their customers. May 2017 Download
Read-across assessment framework (RAAF) - considerations on multiconstituent substances and UVCBs This document describes the additional key issues for the ECHA experts assessing such cases. Such considerations may also be relevant for registrants in the justification of read-across cases. However, due to the case-specific nature of read-across cases for multi-constituent substances and/or UVCBs, the document does not provide considerations on how to deal with the identified issues when adaptations using read-across are developed. March 2017 Download
How ECHA identifies the design for the extended one-generation reproductive toxicity study (EOGRTS) under dossier evaluation The document explains how ECHA identifies and concludes on the design of EOGRTS under dossier evaluation and discusses the crucial information sources for defining the EOGRTS design and triggering the study itself.

The EOGRTS is a modular test method for reproductive toxicity. Its different modules cover the basic study design and separate modules for breeding and assessing a second filial generation, testing for developmental neurotoxicity and developmental immunotoxicity. The appropriate study design needs to be defined, justified and documented. For deciding the need and the study design, a multitude of scientific information needs to be searched and evaluated.
September 2016 Download
Improving the Identification, Evaluation, Adoption and Development of Safer Alternatives Chemical substitution is commonly defined as “the replacement or reduction of hazardous substances in products or processes by less hazardous or non-hazardous substances, or by achieving an equivalent functionality via technological or organisational measures.” It is a longstanding risk management approach in Europe and is a goal of the European Union (EU), Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) regulation. In particular, the authorisation and restriction processes are two important regulatory drivers of substitution within REACH. Substances of very high concern (SVHC) that are made subject to authorisation require an analysis of alternatives to ensure that these highly hazardous substances are progressively replaced by safer alternative substances or technologies where economically and technically feasible. Member State or European Chemical Agency (ECHA) proposals seeking to restrict substances that pose an unacceptable risk to human health and the environment are also required to undergo a Socio Economic Impact evaluation that contains a similar analysis of alternatives process.

In order to improve current working practices in the EU in identifying, evaluating and adopting safer alternatives and to more broadly enhance support for substitution among Member States and the European Commission, ECHA commissioned the Lowell Center for Sustainable Production to undertake a landscape analysis of current capacity and needs. The goal of this project is to identify specific priorities that ECHA and other public authorities could support in the near term in order to advance substitution programs and practices among Member States. A review of select applications for authorisation and restrictions proposals, in addition to surveys and interviews involving industry, Member State and Commission authorities, and NGOs were undertaken to obtain critical insights needed for this research.
August 2016 Download
Analysis of the relevance and adequateness of using Fish Embryo Acute Toxicity test (FET) Test Guideline (OECD 236) to fulfil the information requirements and addressing concerns under REACH ECHA has commissioned a study to gather and analyse the publically available data on fish embryo toxicity (FET), to compare it with available data on standard acute fish toxicity (AFT), and to set up the parameters defining the applicability domain and limitations of a FET test in comparison to AFT. The analysis focused mainly on chemical structure, mode of action and several key physico-chemical characteristics of tested compounds (e.g. solubility, lipophilicity).
The outcome of this analysis constitutes a basis to understand how currently the FET test might be used in the regulatory context of REACH.

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Annex II

Willingness to pay to avoid certain health impacts This study examines the economic benefits of avoiding selected adverse human health outcomes due to exposure to chemicals. May 
Cost and benefit assessments in the REACH restriction dossiers This study describes the costs and benefits of the restrictions included or proposed to be included in Annex XVII of REACH. It summarises and aggregates the information on costs and human health and environmental benefits provided in the restriction dossiers and opinions of the Committees for Risk Assessment (RAC) and Socio-economic Analysis (SEAC). April 
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Usage of (eco)toxicological data for bridging data gaps between and grouping of nanoforms of the same substance. Elements to consider Nanomaterials based solutions have a lot to offer for a wide range of industry sectors from pharmaceuticals to surface technologies. Nanomaterials may be manufactured in several different shapes, sizes and/or with a wide range of surface treatments. Changes made to the particles may not only provide a new function for the nanomaterial but also influence its (eco) toxicological behaviour.
Therefore, a need was identified in 2014 to develop a pragmatic approach for how to ensure safe use of the potentially numerous nanoforms of the same substance under REACH. A nanoform is defined in this document as a composition of a substance that meets the requirements of the EC definition of a nanomaterial. Different nanoforms may differ with regard to size distributions, shape and/or surface chemistry.
Together with RIVM and JRC, ECHA initiated and led a project over 2015 to develop a scientific reference paper to explore the scientific aspects of justifying when and how to use test data from an (eco)toxicity study on one nanoform to cover other nanoforms of the same substance
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Analysis of capacities and capabilities of laboratories to conduct OECD TG 443 extended one-generation reproductive toxicity study ECHA has commissioned a study on global laboratory capacities to conduct extended one-generation reproductive toxicity studies (EOGRTS). In total, 22 laboratories were identified as capable to conduct the studies. Compared with a similar study in 2012, the global laboratory capacity to conduct EOGRTS has increased. January 2016 Download the report
Identification and preliminary analysis of update needs for EUSES ECHA has commissioned RIVM to make a preliminary analysis of the needs for update and improvement of EUSES. The aim of this analysis was to collect, describe and rank various corrections, improvements and extensions of EUSES developed in different contexts over the past years since EUSES 2.1 was released. The report describes possible extensions of the applicability domain for different types of chemicals and model improvements that affect a wider range of chemicals. A ranking for priority of implementation is proposed as part of the report. September 2015 Download the report
Assessment of Reliability of SpERCs
Commissioned by ECHA, this report sets the basis of a framework for assessing the reliability and plausibility of Specific Environmental Release Categories (SpERCs) in the context of REACH information requirements related to the Chemical Safety Assessment. ECHA wants to share the outcome of the project with interested stakeholders and initiate a discussion with industry and Member States competent authorities on the further development of the Best Practice Format proposed by the consultant.
In this report, the consultant proposes Best Practice Format for SpERC factsheets. SpERC factsheets should be streamlined and explanatory information and justifications be provided in a separate background document. The conclusion of the report anticipates the need for further discussion with industry and the Member States to clarify open remaining issues and finalise the Best Practice Format.
The first phase of the project included a thorough overview of the general quality of existing SpERCs and the definition of requisites indicating good quality SpERC factsheet. On this basis a draft Best Practice Format was proposed that has been tested by four industry associations in the second phase of the project. The resulting SpERC factsheet examples are still drafts and therefore are not published in annex to the report. However, as pointed out by the consultant, these factsheets may be further developed by industry and discussed with ECHA and Member States Competent Authorities to provide illustrative examples of factsheets and background documents.
March 2015
2014 CMR Report
In the EU, substances with carcinogenic, mutagenic or reprotoxic properties (CMR substances) should normally have a harmonised classification. At the moment, about 1 400 substances (including substances of unknown or variable composition, complex reaction products or biological materials (UVCB)) and 23 groups of substances (group entries) have a harmonised classification and labelling (CLH) for CMR and are listed in Annex VI to the CLP Regulation.
This report has two aims. Firstly, to see the extent to which registrants and notifiers have classified CMR substances in line with the harmonised classification included in Annex VI (part A) and secondly to see which substances on the EU market are classified for CMR properties by at least some notifiers or registrants but do not currently have a harmonised classification (part B).
January 2015

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Annex III

Annex IV

Report on non-standard methods for assessment of chemicals The Joint Research Centre has published a state-of-the art review of non-animal methods and non-testing (computational) approaches that help promote replacement, reduction, and refinement of animal experiments in the safety assessment of chemicals. The report includes also many "non-standard" methods, e.g. in vitro methods and QSAR modelling that are not included in current regulatory guidelines. The report is of interest for companies that produce or market chemicals and consumer products. It provides a valuable resource for regulatory bodies and non-governmental organisations interested in the use of non-standard methods for enhanced safety testing. The review was completed by the JRC-based European Union Reference Laboratory for Alternatives to Animal Testing (EURL ECVAM)  within a collaboration agreement with ECHA. September 2014 Download the report
Workshop on Compliance Check 2014-2018 – contributing to high quality information for the safe manufacture and use of chemicals 

Proceedings of Workshop on Compliance Check, Helsinki, 31 March - 1 April 2014.

At the workshop, compliance check (CCH) and its strategic direction for the period of 2014-2018 was discussed. The participants included representatives from the Member States and EEA countries; Member State Committee members; two members of the ECHA Management Board Working Group on Planning and Reporting; Member State Committee accredited stakeholder observers representing industry; workers and public interest NGOs; the European Commission; and the ECHA Secretariat.

The workshop found a general agreement that the revised CCH strategy should concentrate on the right substances of concern, those relevant for safe use – both in the selection of substances for compliance checks and for other measures. Furthermore, enhancing interaction with the Member States must be continued to improve efficiency of the CCH process, including its follow-up phase and reporting.

Based on the Workshop conclusions, ECHA will present the key elements for an updated strategy for discussion in the July 2014 CARACAL meeting and will inform the ECHA Management Board meeting accordingly in September.

June 2014 Download the proceedings
Principles for Environmental Risk Assessment of the Sediment Compartment

Proceedings of the Topical Scientific Workshop, Helsinki, 7-8 May 2013

The proceedings reflect the primary objective of the workshop to review the state of art and to contribute to developing updated scientific principles and guidelines for assessing the ecological risks of chemical substances for freshwater and marine sediments. It confirms the significant progress in the last decade that both scientific and regulatory actions have achieved in the scientific understanding of the impact of chemicals on the sediment community.

In the workshop, fruitful discussions on existing gaps and limitations were held; these are addressed and summarised as specific recommendations in the proceedings for each of the three subtopics: Problem definition and conceptual model for sediment risk assessment, exposure and effect assessment.

These recommendations are highly relevant as scientific background in improving the approaches used in different regulatory frameworks both in the EU and internationally, as well as in contributing to the emergence of new or improved approaches that may be applied in the implementation of the REACH, CLP and Biocidal Products Regulations at EU level.
May 2014 Download the proceedings
Service Request on a critical review of the environmental and
physicochemical methodologies commonly employed in the environmental risk assessment of petroleum substances in the context of REACH registrations
This project aimed to provide information on the scientific validity and the general applicability of the Petrotox and Hydrocarbon Block Method tools as developed by CONCAWE for predicting the environmental hazards, exposure and subsequently the environmental risks associated with petroleum hydrocarbons in the context of REACH registrations. The tools are intended to be applicable to any (petroleum) hydrocarbon substance. RIVM was asked by the European Chemicals Agency to review the validity and implementation of the underlying theories and the validity and quality of the QSAR models used to estimate effect and exposure properties of all representative hydrocarbon structures (the so-called CONCAWE library) used to establish reference hydrocarbon blocks. October 2013 Download the report
Mapping Study on Academic Courses Relevant to REACH and CLP The aims of this study are two-fold. Firstly, it aims to identify the number and type of available graduate courses in the fields of REACH and CLP across Europe. Secondly, it is conducted to indicate areas in which input could be provided in order to improve training opportunities for regulatory scientists in the field of chemicals.

The study aims to identify the deficiencies in the current market in terms of REACH and CLP training, and to analyse the duration of the courses that are REACH and CLP specific. It is believed that risk assessment courses should aim to be multidisciplinary in order to cover main areas such as toxicology, environmental fate, ecotoxicology and exposure, as  well as provide practical training programmes with hands-on experience.
April 2013 Download the report
Characterisation, chemical representation and modelling of UVCB substances Substances of unknown or variable composition, complex reaction products or biological materials, collectively called UVCBs under REACH, pose the greatest challenge in a number of REACH processes, in particular in the context of dossier and substance evaluation but also in the priority setting activities of the Agency. The purpose of this contract is to develop a computational methodology for generating representative structures likely to be present in the UVCB and to perform a preliminary screening of their hazardous properties using non-testing methods. The outcome of the project will assist in assessing the homogeneity of UVCBs as far as the likely presence or absence of hazardous constituents is concerned, which can be subsequently applied in dossier and substance evaluation processes but also used by Industry in designing a comprehensive testing strategy of UVCB substances.

The link provides more information on the project, compiled by the developers of the methodology in the Laboratory of Mathematical Chemistry at the Prof. As. Zlatarov University of Bourgas, Bulgaria.
March 2013 Download the report
Report on Survey of Worldwide CROs
Analysis of the results of a survey of 50 CROs which were identified as being potentially able to perform the OECD 443 extended one generation reproductive toxicity study and/or the OECD 488 transgenic rodent somatic and germ cell mutation assay..
September 2012 Download the report
The status of industrial vegetable oils from genetically modified plants The main aims of this report are to: explain the reasons behind the genetic modification of plant oils and explain chemical and biological differences between oils from GMOs and non-GMOs and establish whether it is possible to distinguish them analytically. April 2012 Download the report