UK REACH compliance checklist
- 1 step
Retained EU Law
2006
United Kingdom
UK REACH Regulation (retained EU law)
At a glance
Who this Act binds
Business-side actors with duties under this Act, ranked by how often they appear.
- Manufacturer 37
- Distributor 18
- Any Person 10
- Employer 1
- Trader 1
Plus 30 non-business duties on Crown ministers, regulators, local authorities or tribunals — shown collapsed under each section below.
Step-by-step journeys using this legislation
Walkthroughs that take you from a real business situation to compliance.
Relevant guidance
Practical guides for businesses affected by this Act, ordered by how closely they engage with it.
Direct — cites this Act
2 guidesSupporting — topic alignment
12 guidesCLP Chemical Classification and Labelling
Chemical manufacturer: compliance checklist
Manage solvents, inks and emissions in printing
Ongoing material duties for vehicle manufacturers: end-of-life recycling and restricted substances
Place chemical substances and products on the GB market
Printing business: compliance checklist
Other Acts binding the same actors
For each actor bound by this Act, the other UK Acts that bind them most often. Useful for understanding the full compliance landscape facing each role.
Manufacturers also bound by 472 other Acts (top 5 shown)
- Pressure Equipment (Safety) Regulations 2016 2016 91 duties
- Lifts Regulations 2016 2016 70 duties
- The Ecodesign for Energy-Related Products and Energy Information Regulations 2021 2021 70 duties
- Non-Automatic Weighing Instruments Regulations 2016 2016 67 duties
- Pyrotechnic Articles (Safety) Regulations 2015 2015 64 duties
Distributors also bound by 177 other Acts (top 5 shown)
- The Marketing of Fruit Plant and Propagating Material (England) Regulations 2017 2017 28 duties
- The Marketing of Fruit Plant and Propagating Material (Wales) Regulations 2017 2017 26 duties
- The Marketing of Fruit Plant and Propagating Material Regulations (Northern Ireland) 2017 2017 25 duties
- Electricity Safety, Quality and Continuity Regulations 2002 2002 21 duties
- THE ELECTRICITY SAFETY, QUALITY AND CONTINUITY REGULATIONS (NORTHERN IRELAND) 2012 2012 19 duties
Any Person also bound by 2338 other Acts (top 5 shown)
- Human Medicines Regulations 2012 2012 169 duties
- Merchant Shipping Act 1995 1995 144 duties
- Insolvency (England and Wales) Rules 2016 2016 101 duties
- Road Traffic Act 1988 1988 95 duties
- Air Navigation Order 2016 2016 95 duties
Employers also bound by 694 other Acts (top 5 shown)
- The Income Tax (Pay As You Earn) Regulations 2003 2003 236 duties
- Provision and Use of Work Equipment Regulations 1998 1998 120 duties
- TULRCA 1992 1992 72 duties
- Employment Rights (Northern Ireland) Order 1996 (current NI employment law) 1996 52 duties
- Income Tax (Earnings and Pensions) Act 2003 2003 50 duties
Traders also bound by 826 other Acts (top 5 shown)
- Value Added Tax Regulations 1995 1995 413 duties
- Companies Act 2006 2006 243 duties
- The Large and Medium-sized Companies and Groups (Accounts and Reports) Regulations 2008 2008 114 duties
- Insolvency (England and Wales) Rules 2016 2016 62 duties
- Building Societies Act 1986 1986 56 duties
What this Act requires
Sections that create concrete duties on businesses or carry penalties. Procedural and definitional sections are folded into the “Browse other sections” expander at the bottom of each group. Click any section title to read the source text on legislation.gov.uk.
uri:annex/i/division/0/division/0.10
- Assess case-by-case risks for ozone depletion, photochemical ozone, odour and tainting Manufacturer
uri:annex/i/division/0/division/0.4
- Justify grouping substances together for safety assessment Manufacturer
uri:annex/i/division/1/division/1.3/division/1.3.2
- Explain your decision when you can't decide how to classify a substance Manufacturer
uri:annex/i/division/2/division/2.2
- Justify classification decisions when information is insufficient Manufacturer
uri:annex/i/division/3/division/3.0/division/3.0.3
- Include missing or omitted environmental hazard justifications in chemical safety reports Manufacturer
uri:annex/i/division/3/division/3.2/division/3.2.2
- Justify classification decisions when information is inadequate Manufacturer
uri:annex/i/division/6/division/6.5
- Use assessment data to minimise PBT/vPvB substance risks Manufacturer
uri:annex/ii/part/a/division/0.1
- Compile and provide a compliant safety data sheet for substances or mixtures Distributor
uri:annex/ii/part/a/division/0.2
- Prepare and provide compliant safety data sheets for substances and mixtures Distributor
uri:annex/ii/part/a/division/14/division/14.6
- You must provide transport safety precautions for your chemicals Distributor
uri:annex/ii/part/a/division/16
- Include required information in Section 16 of safety data sheets Distributor
uri:annex/vi/division/1
- Submit registration information with nanoform characterization and justification Manufacturer
uri:annex/vi/division/4
- Compare information needs with available data for nanoforms and identify gaps Manufacturer
uri:annex/vi/division/6/division/1/division/1.2
- Identify joint submission partners in REACH registration Any Person
uri:annex/x/division/9
- Propose further degradation testing if chemical safety assessment requires it Manufacturer
uri:annex/xii/division/1/division/1
- Develop exposure scenarios for unsupported chemical uses Distributor
uri:annex/xii/division/1/division/3
- Produce a Chemical Safety Report with declaration of risk management measures Distributor
uri:annex/xiii/division/2/division/2.1
- Identify PBT/vPvB substances and generate additional data if needed Manufacturer
No data, no market
2 years imprisonment- Register chemical substances before manufacturing or selling them Manufacturer
General obligation to register substances on their own or in mixtures
- Register chemical substances with HSE if you manufacture or import 1 tonne+ per year Manufacturer
Only representative of a non-Great British manufacturer
- Maintaining information as an 'Only Representative' for a foreign manufacturer Any Person
Exemption from the general obligation to register for product and process orientated research and development (PPORD)
- Notify the Agency to exempt R&D substances from full registration Manufacturer
Information to be submitted for general registration purposes
- Submit a technical dossier to register chemical substances Manufacturer
Joint submission of data by multiple registrants
- Submit chemical registration data jointly with other registrants Manufacturer
Information to be submitted depending on tonnage
- Submit chemical safety data based on your annual tonnage Manufacturer
Chemical safety report and duty to apply and recommend risk reduction measures
- Complete a chemical safety assessment and report for substances over 10 tonnes Manufacturer
Registration of on-site isolated intermediates
- Register on-site isolated intermediates with the HSE Manufacturer
Registration of transported isolated intermediates
- Register transported isolated intermediates with the Agency Manufacturer
Joint submission of data on isolated intermediates by multiple registrants
- Submit joint data for isolated intermediates with other registrants Manufacturer
Duties of the Agency
Other duties (1) — Crown / regulator
- Agency must check registration completeness and assign ID numbers Statutory regulator
Further duties of registrants
- Keep your chemical substance registration up to date Manufacturer
Notified substances
- Submit additional chemical data when your tonnage hits the next threshold Manufacturer
Objectives and general rules
- Do not exchange market behaviour information when sharing REACH data Manufacturer
Sharing of existing data in the case of registered substances
- Share chemical safety data with other registrants fairly Any Person
Duty to pre-register for phase-in substances
2 years imprisonment- Pre-register phase-in substances with the HSE Manufacturer
Requirements for safety data sheets
- Provide and update Safety Data Sheets for hazardous substances Distributor
Duty to communicate information down the supply chain for substances on their own or in mixtures for which a safety data sheet is not required
- Provide chemical safety information to customers Distributor
Duty to communicate information on substances in articles
- Inform customers and consumers about hazardous substances in products Distributor
Duty to communicate information on substances and mixtures up the supply chain
- Report new chemical hazards up the supply chain Any Person
Access to information for workers
- Provide workers access to chemical safety information Employer
Obligation to keep information
- Keep all chemical safety and supply information for 10 years Manufacturer
Downstream user chemical safety assessments and duty to identify, apply and recommend risk reduction measures
- Control chemical risks and assess safety for non-standard uses Distributor
Obligation for downstream users to report information
- Report specific chemical uses and safety data to the Agency Distributor
Application of downstream user obligations
- Comply with downstream user chemical safety obligations Distributor
Examination of testing proposals
Other duties (1) — Crown / regulator
- HSE must examine testing proposals and issue a formal decision Statutory regulator
Compliance check of registrations
- Submit information requested by the Agency after a compliance check Manufacturer
Check of information submitted and follow-up to dossier evaluation
Other duties (1) — Crown / regulator
- HSE must review submitted chemical data and follow up on evaluations Statutory regulator
Criteria for substance evaluation
Other duties (1) — Crown / regulator
- HSE must develop and publish a rolling plan for chemical evaluations Statutory regulator
Evaluation of substances on the rolling action plan
Other duties (1) — Crown / regulator
- HSE must ensure evaluation of substances on the rolling action plan Statutory regulator
Requests for further information and check of information submitted
- Submit further information to the Agency by the set deadline Any Person
Follow-up to substance evaluation
Other duties (1) — Crown / regulator
- Health and Safety Executive must conclude and report on substance evaluations Statutory regulator
Registrants' and downstream users' rights
Other duties (1) — Crown / regulator
- Agency must notify you of draft decisions and allow 30 days for comment Statutory regulator
Adoption of decisions under dossier evaluation
Other duties (1) — Crown / regulator
- HSE must issue and notify decisions on dossier evaluations Statutory regulator
Adoption of decisions under substance evaluation
Other duties (1) — Crown / regulator
- Agency must finalize and notify decisions on chemical substance evaluations Statutory regulator
Cost sharing for tests without an agreement between registrants and/or downstream users
- Agree on cost sharing for chemical safety tests Distributor
Publication of information on evaluation
Other duties (1) — Crown / regulator
- The Agency must publish an annual chemical evaluation progress report Statutory regulator
Aim of authorisation and considerations for substitution
- Analyse alternatives and consider substitution for SVHCs Manufacturer
General provisions
- Do not use or sell Annex XIV substances without authorisation Manufacturer
Identification of substances referred to in Article 57
Other duties (1) — Crown / regulator
- Agency must identify and list substances of very high concern Statutory regulator
Granting of authorisations
2 years imprisonmentOther duties (1) — Crown / regulator
- Secretary of State must decide on chemical substance authorisations Crown / Minister / Government department
Procedure for authorisation decisions
Other duties (1) — Crown / regulator
- Agency must provide draft and final opinions on chemical authorisations Statutory regulator
Obligation of holders of authorisations
- Include authorisation numbers on product labels Distributor
Downstream users
- Notify the HSE if you use authorised substances as a downstream user Distributor
Preparation of a proposal
Other duties (1) — Crown / regulator
- HSE must consult the public and businesses on new chemical restrictions Statutory regulator
Agency opinion: risk assessment
Other duties (1) — Crown / regulator
- Agency must provide a risk assessment opinion on proposed restrictions Statutory regulator
Agency opinion: socio-economic analysis
Other duties (1) — Crown / regulator
- Agency must form and publish an opinion on chemical restrictions Statutory regulator
Submission of an opinion to the appropriate authorities
Other duties (1) — Crown / regulator
- Agency must submit and publish opinions on chemical restrictions Statutory regulator
Tasks
Other duties (1) — Crown / regulator
- Agency must provide guidance and technical support to businesses Statutory regulator
Annual report by the Agency to the appropriate authorities
Other duties (1) — Crown / regulator
- Agency must submit annual activity and financial reports for approval Statutory regulator
Qualification and interests
- Experts advising the Agency must declare interests and qualifications Any Person
Conflicts of opinion with other bodies
Other duties (1) — Crown / regulator
- HSE must resolve scientific conflicts with other public bodies Statutory regulator
Duty of confidentiality
- Maintain confidentiality of protected information Any Person
Contacts with stakeholder organisations
Other duties (1) — Crown / regulator
- Health and Safety Executive must engage with stakeholder organisations Statutory regulator
Rules on transparency
Other duties (1) — Crown / regulator
- HSE must establish rules for public access to chemical safety data Statutory regulator
Relations with relevant public bodies
Other duties (1) — Crown / regulator
- The HSE must cooperate with other public bodies to avoid work duplication Statutory regulator
Formats and software for submission of information to the Agency
- Use Agency-specified formats and software for REACH submissions Manufacturer
Reporting
Other duties (1) — Crown / regulator
- Agency must report on REACH operation and non-animal testing Statutory regulator
Electronic public access
Other duties (1) — Crown / regulator
- HSE must provide public online access to chemical substance information Statutory regulator
Communication to the public of information on risks of substances
Other duties (1) — Crown / regulator
- The Agency must provide guidance and inform the public about chemical risks Statutory regulator
Other responsibilities
Other duties (1) — Crown / regulator
- Agency must provide a national helpdesk for REACH advice Statutory regulator
Report
Other duties (1) — Crown / regulator
- HSE must report on UK REACH enforcement and monitoring results Statutory regulator
Statement of reasons for decisions
Other duties (1) — Crown / regulator
- Agency and authorities must provide reasons for REACH decisions Statutory regulator
GENERAL PROVISIONS FOR ASSESSING SUBSTANCES AND PREPARING CHEMICAL SAFETY REPORTS
- Assess chemical safety and prepare safety reports Manufacturer
REQUIREMENTS FOR THE COMPILATION OF SAFETY DATA SHEETS
- Ensure Safety Data Sheets are compiled by a trained, competent person Distributor
INFORMATION REQUIREMENTS REFERRED TO IN ARTICLE 10
- Register chemical substances and provide specific data for nanoforms Manufacturer
GENERAL PROVISIONS FOR DOWNSTREAM USERS TO ASSESS SUBSTANCES AND PREPARE CHEMICAL SAFETY REPORTS
- Assess chemical safety for uses not covered by a Safety Data Sheet Distributor
Application of this Regulation to transferred GB registrations
- Submit required information for transferred GB REACH registrations Manufacturer
Advice from Environment Agency or other environmental regulators to Agency
Other duties (1) — Crown / regulator
- Agency must consult environmental regulators on chemical safety decisions Statutory regulator
Decisions of ECHA relating to existing EU registrations
Amended 3 times- Notify the Agency of existing ECHA decisions Any Person
Existing EU authorisations
Amended 3 times- Submit technical data for existing EU chemical authorisations Trader
Existing applications for EU authorisations
Amended 3 times- Validate and notify the Secretary of State of pending EU REACH authorisations Any Person
Existing Article 7(2) notifications
Amended 3 times- Submit previous EU chemical notifications to the UK Agency Manufacturer
Obligation to keep information
Amended 3 times- Retain chemical safety information for 10 years Any Person
Existing Article 17 registrations
- Provide registration information to HSE for existing on-site isolated intermediates Manufacturer
Existing Article 18 registrations
- Provide information to HSE for grandfathered EU REACH intermediate registrations Manufacturer
Pre-IP completion downstream users and distributors that are to continue to be regarded as downstream users
- If you import chemicals you previously sourced from the EU, provide substance data to HSE Distributor
Protected NI imports
- Notify HSE before importing protected NI chemicals into Great Britain Manufacturer
Browse 271 other sections — procedural / definitional / commencement
uri:annex/i/division/0/division/0.11
uri:annex/i/division/0/division/0.12
uri:annex/i/division/0/division/0.13
uri:annex/i/division/0/division/0.2
uri:annex/i/division/0/division/0.5
uri:annex/i/division/0/division/0.7
uri:annex/i/division/0/division/0.9
uri:annex/i/division/1/division/1.0/division/1.0.3
uri:annex/i/division/1/division/1.0/division/1.0.4
uri:annex/i/division/1/division/1.0/division/1.0.5
uri:annex/i/division/1/division/1.0/division/1.0.6
uri:annex/i/division/1/division/1.1/division/1.1.2
uri:annex/i/division/1/division/1.1/division/1.1.4
uri:annex/i/division/1/division/1.2
uri:annex/i/division/1/division/1.3/division/1.3.1
uri:annex/i/division/1/division/1.4/division/1.4.1
uri:annex/i/division/1/division/1.4/division/1.4.2
uri:annex/i/division/3/division/3.1/division/3.1.2
uri:annex/i/division/3/division/3.1/division/3.1.5
uri:annex/i/division/3/division/3.3
uri:annex/i/division/4/division/4.2
uri:annex/i/division/5/division/5.0
uri:annex/i/division/5/division/5.2/division/5.2.3
uri:annex/i/division/5/division/5.2/division/5.2.4
uri:annex/ii/part/a/division/0.4
uri:annex/ii/part/a/division/0.7
uri:annex/ii/part/a/division/10/division/10.1
uri:annex/ii/part/a/division/10/division/10.2
uri:annex/ii/part/a/division/10/division/10.3
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.1
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.11
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.12
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.4
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.7
uri:annex/ii/part/a/division/11/division/11.1/division/11.1.9
uri:annex/ii/part/a/division/12/division/12.2
uri:annex/ii/part/a/division/12/division/12.5
uri:annex/ii/part/a/division/14/division/14.2
uri:annex/ii/part/a/division/14/division/14.5
uri:annex/ii/part/a/division/14/division/14.7
uri:annex/ii/part/a/division/15/division/15.1
uri:annex/ii/part/a/division/1/division/1.3
uri:annex/ii/part/a/division/2/division/2.1
uri:annex/ii/part/a/division/2/division/2.3
uri:annex/ii/part/a/division/3/division/3.1
uri:annex/ii/part/a/division/3/division/3.2
uri:annex/ii/part/a/division/4/division/4.3
uri:annex/ii/part/a/division/6/division/6.3
uri:annex/ii/part/a/division/7/division/7.1
uri:annex/ii/part/a/division/7/division/7.2
uri:annex/ii/part/a/division/7/division/7.3
uri:annex/ii/part/a/division/8/division/8.1
uri:annex/ii/part/a/division/8/division/8.2/division/8.2.2
uri:annex/ii/part/a/division/8/division/8.2/division/8.2.3
uri:annex/ii/part/a/division/9/division/9.1
uri:annex/ix/division/10
uri:annex/ix/division/9
uri:annex/vi/division/2
uri:annex/vi/division/5/annotations/1
uri:annex/vi/division/6/division/2/division/2.3.7
uri:annex/vi/division/6/division/2/division/2.4.3
uri:annex/vi/division/6/division/2/division/2.4.6
uri:annex/vi/division/6/division/4/division/4.1
uri:annex/vii/division/9
uri:annex/viii/division/9
uri:annex/x/division/10
uri:annex/xi/division/1/division/1.1/division/1.1.1
uri:annex/xi/division/1/division/1.1/division/1.1.2
uri:annex/xi/division/1/division/1.2
uri:annex/xi/division/1/division/1.3
uri:annex/xi/division/1/division/1.4
uri:annex/xi/division/1/division/1.5
uri:annex/xi/division/3
uri:annex/xii/division/1/division/2
uri:annex/xv/division/i
uri:annex/xv/division/ii/division/3/division/1
uri:annex/xv/division/ii/division/3/division/3
uri:annex/xv/division/ii/division/3/division/6
uri:annex/xvii/appendix/7/division/1
uri:annex/xvii/appendix/7/division/2
uri:annex/xvii/appendix/7/division/3/division/3.1
uri:annex/xvii/appendix/7/division/3/division/3.3
uri:annex/xvii/appendix/7/division/5
uri:annex/xvii/appendix/7/division/6
uri:annex/xvii/appendix/7/division/7
Aim and scope
Application
Definitions
General provision
Registration and notification of substances in articles
General requirements for generation of information on intrinsic properties of substances
Substances in plant protection and biocidal products
Duties of ... registrants of substances regarded as being registered
Manufacturing and import of substances
Specific provisions for phase-in substances
Duty to inquire prior to registration
Substance Information Exchange Forums
Sharing of data involving tests
Procedure and time periods for examination of testing proposals
Coherence with other activities
Further information on on-site isolated intermediates
Substances to be included in Annex XIV
Inclusion of substances in Annex XIV
Review of authorisations
Applications for authorisations
Subsequent applications for authorisation
General provisions
Introducing new and amending current restrictions
Restriction decisions
Fees and charges
Establishment and review
Composition
Powers of the Management Board
Composition of the Management Board
Chairmanship of the Management Board
Meetings of the Management Board
Voting of the Management Board
Appointment of the Executive Director
Establishment of the Committees
Establishment of the Forum
Rapporteurs of Committees and use of experts
Establishment of the Board of Appeal
Members of the Board of Appeal
Decisions subject to appeal
Persons entitled to appeal ...
Change of decision where appeal made
Actions before the Court of First Instance and the Court of Justice
The budget of the Agency
Implementation of the budget of the Agency
Combating fraud
Financial rules
Legal personality of the Agency
Liability of the Agency
Privileges and immunities of the Agency
Staff rules and regulations
Languages
Participation of third countries
Participation of international organisations
Scope
Obligation to notify the Agency
Classification and labelling inventory
Harmonisation of classification and labelling
Transitional arrangements
Access to information
Cooperation with other countries and international organisations
Appointment
Cooperation between competent authorities
Tasks of the Member States
Penalties for non-compliance
Free movement
Safeguard clause
Amendments to the Annexes
Implementing legislation
Committee procedure
Preparation of establishment of the Agency
Transitional measures regarding notified substances
Transitional measures regarding existing substances
Transitional measures regarding restrictions
Review
Repeals
Amendment of Directive 1999/45/EC
Entry into force and application
Criteria for substances and, when applicable, for nanoforms thereof, registered...
substances for which it is predicted (i.e. by the application...
At the level of this Annex, the registrant must submit...
Column 1 of this Annex establishes the standard information required...
Without prejudice to the information submitted for other forms, any...
In addition to these specific rules, a registrant may propose...
Before new tests are carried out to determine the properties...
When, for certain endpoints, it is proposed not to provide...
Column 1 of this Annex establishes the standard information required...
Without prejudice to the information submitted for other forms, any...
In addition to these specific rules, a registrant may adapt...
Before new tests are carried out to determine the properties...
When, for certain endpoints, information is not provided for other...
Column 1 of this Annex establishes the standard information required...
non-phase-in substances manufactured or imported in quantities of 1 to...
Any other relevant physicochemical, toxicological and ecotoxicological information that is...
Column 2 of this Annex lists specific rules according to...
Without prejudice to the information submitted for other forms, any...
In addition to these specific rules, a registrant may adapt...
Before new tests are carried out to determine the properties...
When, for certain endpoints, information is not provided for other...
Any other relevant physicochemical, toxicological and ecotoxicological information that is...
This Annex lays down the criteria for the identification of...
For the identification of PBT substances and vPvB substances a...
A weight-of-evidence determination means that all available information bearing on...
The information used for the purposes of assessment of the...
The identification shall also take account of the PBT/vPvB-properties of...
This Annex shall apply to all organic substances, including organo-metals....
Annexes VII to X set out the information requirements for...
one tonne or more in accordance with Article 12(1)(a), 10...
In addition to the specific rules set out in column...
The requirements specific to nanoforms in this Annex are without...
At the level of this Annex, the registrant must submit...
Column 1 of this Annex establishes the standard information required...
Without prejudice to the information submitted for other forms, any...
In addition to these specific rules, a registrant may propose...
Before new tests are carried out to determine the properties...
When, for certain endpoints, it is proposed not to provide...
Entry 72 — restricted substances and maximum concentration limits by...
annex/XVII/appendix/3/paragraph/1
ANNEX XVII Table 2: rows 1 - 50
ANNEX XVII Table 2: rows 51 - 100
ANNEX XVII Table 2: rows 101 - 150
ANNEX XVII Table 2: rows 151 - 200
ANNEX XVII Table 2: rows 201 - 250
ANNEX XVII Table 2: rows 251 - 300
ANNEX XVII Table 2: rows 301 - 332
ANNEX XVII Table 3: rows 1 - 50
ANNEX XVII Table 3: rows 451 - 500
ANNEX XVII Table 3: rows 501 - 550
ANNEX XVII Table 3: rows 551 - 600
ANNEX XVII Table 3: rows 601 - 650
ANNEX XVII Table 3: rows 651 - 700
ANNEX XVII Table 3: rows 701 - 750
ANNEX XVII Table 3: rows 751 - 800
ANNEX XVII Table 3: rows 801 - 829
ANNEX XVII Table 3: rows 51 - 100
ANNEX XVII Table 3: rows 101 - 150
ANNEX XVII Table 3: rows 151 - 200
ANNEX XVII Table 3: rows 201 - 250
ANNEX XVII Table 3: rows 251 - 300
ANNEX XVII Table 3: rows 301 - 350
ANNEX XVII Table 3: rows 351 - 400
ANNEX XVII Table 3: rows 401 - 450
ANNEX XVII Table 4: rows 1 - 50
ANNEX XVII Table 4: rows 51 - 100
ANNEX XVII Table 4: rows 101 - 150
ANNEX XVII Table 4: rows 151 - 200
ANNEX XVII Table 4: rows 201 - 250
ANNEX XVII Table 4: rows 251 - 300
ANNEX XVII Table 4: rows 301 - 350
ANNEX XVII Table 4: rows 351 - 400
ANNEX XVII Table 4: rows 401 - 429
ANNEX XVII Table 6: rows 1 - 50
ANNEX XVII Table 6: rows 51 - 100
ANNEX XVII Table 6: rows 101 - 150
ANNEX XVII Table 6: rows 151 - 200
ANNEX XVII Table 6: rows 201 - 241
This Annex outlines the information that may be addressed by...
The Agency shall prepare guidance for the preparation of SEAs....
However, the level of detail and scope of the SEA,...
An SEA may include the following elements:
impact of a granted or refused authorisation on the applicant(s),...
Application of Article 127G to qualifying Northern Ireland goods
Appointment of only representative where Article 127E applies
Authorisations and imports from Northern Ireland
Authorisations and qualifying Northern Ireland goods
CRITERIA FOR SUBSTANCES REGISTERED IN QUANTITIES BETWEEN 1 AND 10 TONNES
CRITERIA FOR THE IDENTIFICATION OF PERSISTENT, BIOACCUMULATIVE AND TOXIC SUBSTANCES, AND VERY PERSISTENT AND VERY BIOACCUMULATIVE SUBSTANCES
DOSSIERS
EXEMPTIONS FROM THE OBLIGATION TO REGISTER IN ACCORDANCE WITH ARTICLE 2(7)(b)
Existing Article 9 exemptions
Existing authorised downstream users under EU law
Existing EU registrations which have effect as GB registrations
Existing examinations of testing proposals
GENERAL RULES FOR ADAPTATION OF THE STANDARD TESTING REGIME SET OUT IN ANNEXES VII TO X
Import from Northern Ireland where Article 127E applies
Interpretation of Articles 127A to 127C
LIST OF SUBSTANCES SUBJECT TO AUTHORISATION
Notification by Northern Irish supplier where Article 139A applies
Post-IP completion periods used in this Title
Registrations under Article 127L and Article 127M
Regulations under this Regulation
RESTRICTIONS ON THE MANUFACTURE, PLACING ON THE MARKET AND USE OF CERTAIN DANGEROUS SUBSTANCES, MIXTURES AND ARTICLES
SOCIO-ECONOMIC ANALYSIS
STANDARD INFORMATION REQUIREMENTS FOR SUBSTANCES MANUFACTURED OR IMPORTED IN QUANTITIES OF 100 TONNES OR MORE
Substances of very high concern: sunset dates and latest application dates
The Agency
The consent requirement
Official guidance
Authoritative sources published by regulators or government explaining this legislation.
- Export Control Joint Unit — guidance (opens in a new tab) from ECJU Detailed Guidance
- End-of-life vehicles — producer responsibility guidance (opens in a new tab) Detailed Guidance
- HSE: UK REACH (opens in a new tab) from HSE Detailed Guidance
- HSE: Wood dust guidance (opens in a new tab) from HSE Detailed Guidance
- HSE: Cement health risks (opens in a new tab) from HSE Detailed Guidance
- Notifying substances in articles - HSE (opens in a new tab) from HSE Detailed Guidance
- SVHCs overview - HSE (opens in a new tab) from HSE Detailed Guidance
- UK REACH Candidate List of SVHCs - HSE (opens in a new tab) from HSE Detailed Guidance
- UK REACH roles explained - HSE (opens in a new tab) from HSE Detailed Guidance
- DUIN notifications for downstream users and distributors - HSE (opens in a new tab) from HSE Detailed Guidance
- ... and 39 more
Enforcement and responsible bodies
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HSE
PrimaryHealth and Safety Executive
Workplace health, safety, and welfare regulation across all industries. Enforces the Health and Safety at Work Act 1974 and related regulations. Investigates …
Office for Environmental Protection
Independent body established post-Brexit to scrutinise environmental law and investigate complaints about public authorities' failures to comply with environmental law in England …
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