The importance of REACH registration data for authorities

Similar documents
9/10/2013. Contributions of ECHA to the achievement of the REACH goals. Content of Discussion

REACH/CLP Update. Roseleen Murphy IMFI 12 th May 2011

ECHA and the implementation of REACH,CLP and other tasks

Hazard Communication. Hazard Communication

Update from ECHA. REACH Implementation Workshop X. 13 December Laurence Hoffstadt ECHA Substance Identification & Data Sharing

April 21 st, 2016 Webinar. registrations What is next for the industry?

Guidance on Scientific Research and Development (SR&D) and Product and Process Orientated Research and Development (PPORD)

ASSESSMENT OF THE CONSOLIDATED ANNUAL ACTIVITY REPORT OF THE AUTHORISING OFFICER FOR THE YEAR 2014

SDS and what is new under REACH and EU GHS? PRISM2 Workshop Promoting Resposibility in SME s 08 April Slovakia. L. Heezen

Intertek Health, Environmental & Regulatory Services

CLP the implementation of GHS in the EU Facts and practical advice

Implementation of REACH & CLP: common challenges of national authorities and ECHA

REACH Evaluation. Graham Lloyd Regulatory/Technical. REACH in Practice Conference 1 June, Steptoe & Johnson LLP & Regulatory Compliance Ltd

Guidance on the preparation of dossiers for harmonised classification and labelling (CLH) under Regulation (EC) No.

State of play on the candidate list. of Substances of Very High Concern

Background to CLP. Presentation Overview. Why Introduce GHS? Basic CLP requirements 8/30/2011

1. Address by Dr. Chris SAID, Parliamentary Secretary for Consumers, Fair Competition and Public Dialogue

REACH and CLP an industrial perspective on registrations and notifications

REPORTING OF REACH IMPLEMENTATION

Future road of REACH. Checking out the map. Fulvia Raffaelli Unit G.1 : Chemicals, REACH. European Commission Enterprise and Industry

REACH Pre-registration Questions and Answers

FORUM FOR EXCHANGE OF INFORMATION ON ENFORCEMENT. Disclaimer:

Multi-Annual Work Programme

Procedure for handling applications for authorisation and review reports under REACH

The Classification and Labelling Inventory. Cefic s viewpoint

Health and Safety Authority. Function and Scope of REACH and CLP Helpdesks

Europe Direct is a service to help you find answers to your questions about the European Union.

VLARIP Netwerkevent. 24 januari 2013

CLP Regulation Recent implementation and issues. Workshop "Product Stewardship and PROCESS SAFETY 30/11/2017 Dr. Blanca Serrano

Strategies for REACH Compliance. Chicago 23 March 2012

Agenda. Workflows and Software Tools for the Process of Registration, Evaluation, Authorisation and Restriction of European Chemicals

MINIMUM CRITERIA FOR REACH AND CLP INSPECTIONS 1

Regulatory fitness check of chemicals legislation

REACH Forum, Compliance Control of REACH and CLP Regulations

Second REACH registration deadline a success. 3 Nearly more substances registered by industry. 10 Setting scientific. 14 Promoting substitution

Harmonisation of Information for Poison Centres

Bilateral screening: Chapter 27 PRESENTATION OF THE REPUBLIC OF SERBIA Classification, labelling and packaging of substances and mixtures - CLP

CHEMICALS (Classification, Labelling, Packaging of substances and mixtures -CLP) Screening Meeting EU Serbia June 2013

Practical guide 7: How to notify substances in the Classification and Labelling Inventory

REPUBLIC OF SERBIA Bilateral screening: Chapter 1 Free Movement of Goods. C L P Classification, Labeling and Packaging of substances and mixtures

ITMA 2015 Textile Colourant & Chemical Leaders Forum. Updates on REACH Regulation. Dr Maurizio Colombo, REACH and CPL Coordinator, Federchimica

Update of the Work plan on international activities 2012

LISAM SYSTEMS REACH Compliant SDSs: What s Changed and What s Coming

REACH-IT Industry User Manual

From pre-registration to joint submission Hendrik Abma Director General European Association of Chemical Distributors (FECC)

Guidance on the Biocidal Products Regulation

Final Draft Agenda Sixteenth meeting of the Forum for Exchange of Information on Enforcement (Forum-16) October 2013

Guidance on the Biocidal Products Regulation

Changes to Chemical Labels and SDS - Speaker s notes

CHEMICAL WATCH GLOBAL ENFORCEMENT SUMMIT 2015

EU harmonization of the information for emergency health response (Art. 45 Regulation 1272/2008 )

EU Poison Centres Webinar. 27 May 2014, 9:00am BST

A look into the PCN format, UFI generator and EU PCS

Biocidal product regulation the changes to come

Newsletter September 2017

essenscia SME projects to improve REACH & CLP implementation: VLARIP & WALRIP

Global REACH legal services

Guidelines on Occupational Safety and Health Management Systems Ministry of Labour Notification No. 53, April 30, 1999

REACH 2018 registration deadline Last advice for companies

Confirmation Letter of REACH Registration

Questions and answers about Recycling Processes

HAZARDOUS SUBSTANCES POLICY Page 1 of 5 Reviewed: May 2017

EUROPEAN PARLIAMENT Committee on the Environment, Public Health and Food Safety

Introduction UN GHS. CLP outline. Requirement for SDS. Measures needed GHS CLP SDS. Transition from DSD/DPD to CLP DSD/DPD CLP

EUROPEAN COMMISSION DIRECTORATE-GENERAL FOR ENERGY

Novità in materia di CLP : impatto sui biocidi. Maristella Rubbiani CSC/ISS

Continuous Professional Development of Health Professionals European Context

DRAFT OPINION. EN United in diversity EN. European Parliament 2018/0018(COD) of the Committee on Industry, Research and Energy

Helpdesk report 2016 (art. 24 REACH)

PMR PROJECT IMPLEMENTATION STATUS REPORT (ISR)

Safety. 3.1 The Law Affecting Health and Safety in the UK UK Health and Safety at Work Act (HASWA) Statutory Duties of the Employer

COSHH - Fundamentals of Risk Assessment and Control Qualification specification

Patient Registry Initiative- Strategy and Mandate of the Cross-Committee Task Force

Q:\COMP\ENVIR2\PPA90 POLLUTION PREVENTION ACT OF 1990

MEDICINES CONTROL COUNCIL

III-V Materials, KETs and CLP/REACH Procedures

Agency Mission Assurance

IVDD revision changes to the European regulation of in-vitro diagnostic (IVD) Medical Devices. Med-Info. TÜV SÜD Product Service GmbH

Final Minutes. Minutes of the 12th Meeting of the Member State Committee (MSC-12) 9-10 June 2010

Promoting SCP patterns through the use of the voluntary, market-based EU Eco-Management and

Value Added Medicines Rethink, Reinvent & Optimize Medicines, Improving Patient Health & Access

Global Market Expansion Services for Safety, Environment, Quality, and Regulatory Affairs (SEQRA)

320- HAZARD COMMUNICATION

EUROPEAN COMMISSION DIRECTORATE-GENERAL ENVIRONMENT Directorate A Green Economy ENV.A.3 - Chemicals

The implementation of the Clinical Trial Regulation (CTR, n 536/2014) in Belgium. and impact on the ethical review process

Personal Protective Equipment Program. Risk Management Services

Certification Scheme for a Certificate of Pharmaceutical Product (CPP) IFPMA CPP Network Training Toolkit

Amendments to Part II of the Canada Labour Code. October 24, 2014

( ) Page: 1/24. Committee on Subsidies and Countervailing Measures SUBSIDIES

COMMISSION OF THE EUROPEAN COMMUNITIES

COMMISSION OF THE EUROPEAN COMMUNITIES

Use of disease registries for benefitrisk evaluation of medicines: A regulatory perspective. DIA Europe April Basel, Switzerland

Food Standards Agency in Wales

ZAMBIA MEDICINES REGULATORY AUTHORITY EMPLOYMENT OPPORTUNITY

Commission Guidelines for the implementation of the Clinical Trials Regulation NTA Ethics Oslo

Department of Defense INSTRUCTION

CHABOT/LAS POSITAS COMMUNITY COLLEGE DISTRICT

Health & Safety and Wellbeing Policy

WARTBURG COLLEGE ENVIRONMENTAL AND OCCUPATIONAL SAFETY PROGRAM. Hazardous Chemical Communication Plan (Worker Right To Know)

Guide to Incident Reporting for General Medical Devices and Active Implantable Medical Devices

Transcription:

German Environment Agency REACH Compliance workshop The importance of REACH registration data for authorities Lars Tietjen

Content REACH Substances Selection of candidates for further work Registration data Outlook 21.09.2018 2

Communication in the supply chain M/I SDS Manufacturer (substance) SDS Formulator SDS SDS Distributor?? Professional user Registration CSR Technical Dossier >1 t/a CSR Chemical Safety Report >10 t/a 3 Information on uses, hazards Exposure scenario Hazard substance; PBT; vpvb [>10 t/a] 21.09.2018 3

REACH regulation Recital 14 This Regulation will generate information on substances and their uses. Available information, including that generated by this Regulation, should be used by the relevant actors in the application and implementation of appropriate Community legislation, for example that covering products, and Community voluntary instruments, such as the eco-labelling scheme. The Commission should consider in the review and development of relevant Community legislation and voluntary instruments how information generated by this Regulation should be used, and examine possibilities for establishing a European quality mark. Recital 21 Although the information yielded on substances through evaluation should be used in the first place by manufacturers and importers to manage the risks related to their substances, it may also be used to initiate the authorisation or restrictions procedures under this Regulation or risk management procedures under other Community legislation. Therefore it should be ensured that this information is available to the competent authorities and may be used by them for the purpose of such procedures. 21.09.2018 4

Authorities Support actors (ECHA, MSCAs) Receive and manage registrations (ECHA) Dossier Evaluation (ECHA, MSCAs) Substance Evaluation (MSCAs, ECHA) Propose further action on chemicals (ECHA, MSCAs, other authorities) Inform the public (COM, ECHA, MSCAs) 21.09.2018 5

Substances Ca. 145.000 substances in C+L inventory Ca. 21.500 registered substances [+? exempted from registration (polymers etc.)] 352 Substances on CoRAP; 452 in PACT 21.09.2018 6

SVHC Roadmap The starting point remains the Commissioners' commitment to identify and include in the candidate list all SVHCs, relevant for the European Union, by the end of 2020. 7

Selection of substances for further work Registered substances+other relevant substances substances for further work for authorities 21.09.2018 8

Possible regulatory action REACH CLP WFD IED Restriction SVHC Identification Authorisation WFD=Water Framework Directive IED=Industrial Emissions Directive 21.09.2018 9

Selection of substances for further work Registered substances+other relevant substances Hazard information; information on uses, possible exposure substances for further work for authorities 21.09.2018 10

Screening (Information used) Data from Registration Monitoring Research Projects (external) Published Data Research Projects (internal) QSAR; SAR Groups of Substances Internal Databases (UBA) 21.09.2018 11

Manual Screening Source ECHA 2018 21.09.2018 12

REACH registration data Very much data on substances is available publicly and additional date for authorities 21.09.2018 13

REACH registration data - observations Hazard Information not enough data to decide on SVHC properties P/vP or B/vB accepted from registrant additional data needed for SVHC identification? documentation of (Q)SAR, read-across limited long-term ecotoxicity data, bioaccumulation simulation studies on degradation Exposure Information limited information on downstream uses exposure assessment sometimes difficult to assess real data on volumes used missing (only generic information) 21.09.2018 14

Outlook (1/2) REACH Review/COM Art. 117 report: Action 1: Encourage updating of registration dossiers The Commission in collaboration with ECHA, Member States and industry will identify why registrants are not updating their dossiers and make proposals for improvements by first quarter 2019, as appropriate. Action 2: Improve evaluation procedures ECHA is requested to significantly increase the efficiency of the evaluation procedures by 2019 by: (1) identifying the main reasons for non-compliance of registration dossier and developing remedies; (2) where appropriate, applying the various evaluation procedures in parallel; (3) systematically implementing a grouping approach, where this is possible; (4) improving work-sharing across evaluation activities with Member States; and (5) improving decision-making procedures. Action 16: Review of registration requirements for low tonnage substances and polymers The Commission will further investigate information necessary to assess the affordability of additional information requirements for low tonnage substances or to identify relevant polymers that could be subject to registration. 21.09.2018 15

Outlook (2/2) Percentage of Dossier evaluations by ECHA Article 41 Compliance check of registrations [ ] 5. To ensure that registration dossiers comply with this Regulation, the Agency shall select a percentage of those dossiers, no lower than 5 % of the total received by the Agency for each tonnage band, for compliance checking. The Agency shall give priority, but not exclusively, to dossiers meeting at least one of the following criteria: [ ] 7. The Commission may, after consulting with the Agency, take a decision to vary the percentage of dossiers selected and amend or include further criteria in paragraph 5 in accordance with the procedure referred to in Article 133(4). Registrants should improve and update the dossiers when needed Authorities should support actors and help to improve guidance, tools etc. 21.09.2018 16

Thank you for your attention! Lars Tietjen lars.tietjen@uba.de Tel.: +49 (0)340-2103-3111 https://www.umweltbundesamt.de/en/topics/chemicals 21.09.2018 / Hier steht der Veranstaltungstitel in 12 Punkt 17