Member States Reporting under REACH art. 117 / CLP art.46

Transcription

1 Case Id: cb7582fa-cc3e-4b77-a6e4-f7dcab9b17cd Date: 11/06/ :55:08 Member States Reporting under REACH art. 117 / CLP art.46 Fields marked with are mandatory. Introduction General Information Please note that depending on what your answers are throughout the questionnaire, hidden questions may show up, so please disregard the numbering in case it does not follow a logic order. A glossary is available in the section 'background document'. 1.Which Member State are you reporting for? Croatia 2. Primary contact person's name Dubravka Marija Kreković 3. Please provide an address for the primary contact person dubravkamarija.krekovic@miz.hr Theme 1 - Information on the Competent Authority 4. Please explain how Competent Authorities are organised for the operation of REACH in your country? (Please note that this Section does not include information on enforcement authorities that will be covered under Theme 9 on enforcement) 1

2 5. How many Competent Authorities are responsible for REACH? A description of each Competent Authority will be asked in the following sections. Similar series of questions corresponding to the number of Competent Authorities you enter will appear below. 1 One / First Competent Authority Responsible for REACH 6. What is the name of the Competent Authority? Ministry of Health 7. What is the address of the Competent Authority? Zagreb, Ksaver 200a 8. What is the address of the Competent Authority? helpdesk-reach@miz.hr 9. What is the telephone number of the Competent Authority? What part of REACH does this part of the Competent Authority deal with? Please choose one or more answers. All Evaluation Risk Assessment Helpdesk Authorisation Restriction Registration Other 2

3 11. From what part of Government does this part of the Competent Authority have authority from? Please choose one or more answers. Environment Occupational Health and Safety Public Health Consumer Protection Economy/Industry Other 12. Please specify the number of staff of the Competent Authority working on the implementation of REACH: Do you have specialised staff in the following categories? Please quantify these skills in FTE (Full Time Equivalent). For a definition of Full Time Equivalent, please refer to the glossary. FTE Toxicologist 0 Ecotoxicologist 0 Chemist 1 Exposure Assessor 0 Risk Assessor 0 Risk manager 0 Economist 0 IT 0 Communication 0 Other Is the level of expertise of the Competent Authority adequate to deal with all requirements under REACH?, we have good coordination with other Institutes in country 3

4 15. Are the staff of the REACH Competent Authority involved in other chemical legislation? 16. What other chemical legislation are the staff of the REACH Competent Authority involved in? Please choose one or more answers. PIC Regulation Food legislation Workers Protection legislation Cosmetics Medical devices Biocides CLP Pesticides POPs Other 17. Are there any other institutions (agency, institute, regional authorities) that the Competent Authority works with in relation to REACH issues? If, please list the other institutions that the Competent Authority works with: Croatian Institute for Toxicology and Antidoping, Institute for Medical Research and Occupational Health, Croatin Institute for Public Health 18. Does the Competent Authority outsource any of its work? 4

5 19. Does the Competent Authority have appropriate financial resources? 1 = Very low (not appropriate at all); 2 = Low (of some relevance but not of any great significance); 3 = Medium (reasonably appropriate); 4 = High (highly appropriate); 5 = Very high (completely appropriate) Does the Competent Authority have appropriate technical resources (understood in terms of expertise, skills and competences of the staff)? Does the Competent Authority have appropriate human resources (understood in terms of number of staff)? Space is available below to provide further comments on the resourcing of the Competent Authority. Theme 2: Information on cooperation and communication with other Member States, the European Chemicals Agency (ECHA) and the Commission 5

6 23. How could the communication and collaboration for REACH between Member States be improved? The communication and collaboration between MS should be improved in way to make much faster agreement between issues which are in the most interest for all MS 24. How could the collaboration with other agencies in your country be improved? The main problem that we (CA and other agencies) don't have enought stuff. Even we don't have enough working stuff, collaboration with other agencies is very good. 25. How could the communication and collaboration with ECHA be improved? We don't see any problems regarding communicaton and collaboration with ECHA 26. How could the exchange of information and dialogue between Member States and the Commission be improved? The process is sometimes very slow, and the documnts are sent often in a laste minute Theme 3: Operation of the national helpdesk 6

7 27. Please provide the name of the organisation(s) responsible for operating the Helpdesk(s) for REACH. Ministry of Health 28. What is (are) the address(es) of the Helpdesk(s)? Croatia, Zagreb, Ksaver 200a 29. What is (are) the web page address(es) of the Helpdesk(s)? What is (are) the address(es) of the Helpdesk(s)? 31. What is (are) the telephone number(s) of the Helpdesk(s)?

8 32. What is the institutional structure of the Helpdesk(s)? Separate independent entity(ies) Part of Competent Authority Part of business association/chamber of commerce Other 33. Please quantify these skills in FTE (Full Time Equivalent). FTE Toxicologist 0 Ecotoxicologist 0 Chemist 1 Exposure Assessor 0 Risk Assessor 0 Risk manager 0 Economist 0 IT 0 Communication 0 Other Is the level of expertise adequate to respond to all enquiries? 35. For which topics does the national helpdesk feel it necessary to refer the enquirer to the ECHA helpdesk? Since we entered to EU in July 2013, we had lots of question regarding registration since we had transitional period for Croatian companies 8

9 36. What are the services offered by the Helpdesk? Please choose one or more answers. Website Newsletter Advice services Trainings Mediation / conflict resolution Other 37. In which language(s) are these services accessible? croatian, english 38. Is the same Helpdesk used to provide help to Industry on CLP? 39. Does the Helpdesk receive any non-governmental support? 40. Please describe the Helpdesk quality assurance mechanisms: ISO Is ISO9000 norm in place? 9

10 42. How many enquiries does the Helpdesk receive per year? > How are the majority of enquiries received? Please choose one or more answers. Phone Fax Letter Other information 44. Do you provide specific advice to SME's? If yes, please specify how this advice is customized for the needs of SMEs. In cooperation with Croatian Chamber of commerce 10

11 45. What is the company size of enquirers? (please specify the percentage of the total each of them represent) If no information is available for a specific type of company, please indicate N/A in the corresponding box. % Large enterprises Medium enterprises Small enterprises Micro enterprises Other N/A N/A N/A N/A N/A 46. For each type of enquiry received, please provide the percentage of the total number of enquiries during the reporting period: Pre-registration Please insert a figure. The individual percentages should add up 100% altogether. 5 % Registration 7 % Evaluation 1 % Authorisation 1 % Restriction 3 % Testing (Information requirement/registration) 0 % Data sharing 0 % 11

12 Enforcement 20 % CSR preparation 0 % CLP Classification 10 % CLP Labelling 10 % CLP Packaging 5 % CLP Classification and labelling inventory 3 % SIEFs 0 % REACH-IT 0 % IUCLID5 0 % Downstream user obligations 5 % 12

13 Only representative obligations 1 % Obligations regarding articles 1 % Safety Data Sheets 20 % SVHC 1 % Other 7 % 47. Are enquiries received mostly: 'Straight-forward' is understood as those enquiries that can be answered without performing any prior research. 'Complex' is understood as those enquiries that require a minimum level of research before been answered or that demand exhaustive elaboration. Complex Straightforward information 48. What proportion of enquiries received are deemed to be: 1) straight forward Please provide an approximate estimation as an average per year. The individual percentages should add up 100% altogether. 35 % 2) complex 65 % 13

14 49. How long, on average, does it take to respond to the following types of questions? 4 hours 1 day 3 days 1 week 2 weeks > 2 weeks info Straight forward questions Complex questions 50. Are any types of enquiry outsourced? 51. What types of enquiry are outsourced? Please choose one or more answers. Pre-registration Registration Evaluation Authorisation Restriction Testing Enforcement CSR preparation CLP SIEFs REACH-IT IUCLID5 Downstream user obligations Obligations regarding articles Safety Data Sheets SVHC Other (please list) 52. Does the Helpdesk seek feedback on its performance? 53. Does the Helpdesk review its performance and consider ways to improve its effectiveness? 14

15 If yes, what were the measures taken to improve its effectiveness? We prepared new operative procedures 54. How could the cooperation between Helpdesks under Helpnet be improved? The cooperation between Heldesks could be improved with more meetings or at least webinars 55. How could the cooperation between Helpdesk outside Helpnet be improved? It wolud be improved in regional level. Neigbouring countries have similar problems 56. How frequently do you use HelpEx? Daily Weekly Monthly Less frequently Theme 4: Awareness raising activities 57. Has the Member State carried out any specific awareness raising activities? 15

16 58. What types of activities have been carried out? Please choose one or more answers. Television spots Articles in Newspapers Radio spots Speaking events Information seminar Telephone surveys Leaflets and newsletters Articles in industry magazines Website / Social Media Other 59. Who is the target audience for your awareness raising activities? Please choose one or more answers. Consumers directly Consumers indirectly through multipliers (media, associations etc) SME in downstream sectors All companies in downstream sectors SMEs in chemicals sector All companies in chemicals sector Other 60. Please describe how the information was adapted for the specific target audience: With good cooperation with Chameber of Commerce 16

17 61. How effective was each type of activity? 1 = Very low (not appropriate at all); 2 = Low (of some relevance but not of any great significance); 3 = Medium (reasonably appropriate); 4 = High (highly appropriate); 5 = Very high (completely appropriate) If you have not ticked an activity in question 59, please state N/A N/A Television spots Articles in Newspaper Radio spots Speaking events Information seminar Telephone surveys Leaflets and newsletters Articles in industry magazines Websites / social media Other 62. Do you measure the effectiveness of the activities? 64. Do you have a REACH webpage/website? Theme 5: Information on the promotion of the development, evaluation and use of alternative test methods 17

18 67. Does the Member State contribute to EU and/or OECD work on the development and validation of alternative test methods by participating in relevant committees? 68. What has been the overall public funding on research and development of alternative testing in your Member States each year? Euros 0-10,000 Euros 10, ,000 Euros 100,001-1,000,000 More than Euros 1, 000, 000 information 69. Please mention other relevant activities carried out on information on the Promotion of the Development, Evaluation and Use of Alternative Test Methods: Theme 6: Information on participation in REACH Commission and ECHA expert groups / committees (Forum, REACH Committee, MSC, RAC, SEAC, CARACAL, RCN, Helpnet) 70. How effective is the work of the FORUM Committee? 1 = Very low (not appropriate at all); 2 = Low (of some relevance but not of any great significance); 3 = Medium (reasonably appropriate); 4 = High (highly appropriate); 5 = Very high (completely appropriate)

19 71. Please specify if needed: 72. How could the effectiveness be improved? 73. How effective is the work of the REACH Committee? Please specify if needed: 75. How could the effectiveness be improved? 19

20 76. How effective is the work of the Member States Committee (MSC)? Please specify if needed: 78. How could the effectiveness be improved? 79. How effective is the work of the Risk Assessment Committee (RAC)? Please specify if needed: 20

21 81. How could the effectiveness be improved? 82. How effective is the work of the Socio-Economic Committee (SEAC)? Please specify if needed: 84. How could the effectiveness be improved? 85. How effective is the work of the CARACAL (Competent Authorities for Reach and CLP)?

22 86. Please specify if needed: 87. How could the effectiveness be improved? 88. How effective is the work of the Risk Communication Network (RCN)? Please specify if needed: 90. How could the effectiveness be improved? 22

23 91. How effective is the work of the HelpNet Committee? Please specify if needed: 93. How could the effectiveness be improved? Theme 7: Information on Dossier Evaluation and Substance Evaluation activities Dossier evaluation 94. Has the Member State been involved in Dossier evaluation within the reporting period? Substance evaluation 102. Has the Member State been involved in substance evaluation within the reporting period? 23

24 Theme 8: Annex XV Dossiers (restriction and identification of SVHC) and other points related to the identification of SVHC Annex XV Restriction Dossiers 115. Has the Member State been involved in the preparation of Annex XV Restriction Dossiers within the reporting period? Annex XV SVHC Dossiers 131. Has the Member State been involved in the preparation of Annex XV SVHC Dossiers? Other points related to the identification of SVHC 145. Do you consider that there is enough coordination between ECHA and Member States during the implementation of the SVHC Roadmap? 146. What were the financial and human resources dedicated to SVHCs identification (both screening and preparation of an Annex XV dossier) before and after the agreement on the SVHCs Roadmap in March 2013? Theme 9: Information on REACH enforcement activities General information 24

25 147. Please explain how the enforcement of REACH is organised in your country; please concentrate on the changes from the last reporting: For a definition of 'enforcement', please refer to the glossary. National enforcement authority in Republic Croatia is Ministry of Health. Health Improvement Directorate Are the national enforcement authority(ies) in charge of REACH, only dealing with REACH? If, what are their additional responsibilities? NEA is all dealing with food safety, GMO, noise 149. Describe the general status of the resources allocated to enforcing authorities for tasks related to the enforcement of REACH (assessment of annual budget and staff): 4 inspectors on national level 30 inspectors on regional level no data regarding annual budget Enforcement Strategy(ies) General information on the enforcement strategy (or strategies) in place within the Member State 150. Has an overall strategy been devised and implemented for the enforcement of REACH? For a definition of 'enforcement', please refer to the glossary. devised implemented 25

26 151. Is(are) the strategy(ies) in line with the strategy devised by the Forum? Forum strategy as described in the document Strategies for enforcement of Regulation (EC). 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC). 1272/2008 on the classification, labelling and packaging of substances and mixtures (CLP) as adopted at the 9th meeting of the Forum on 1-3 March Please outline the enforcement strategy within the Member State: According to annually plan of sanitary inspection 153. What type of activities does this strategy entail? advice, inspection, penalties 154. Is this enforcement strategy publicly available? Inspection strategy 156. Describe the REACH inspection strategy: For a definition of 'inspection', please refer to the glossary. 26

27 157. How has the inspection strategy evolved from 2010 to 2014? Croatia entered EU in July 2013, and we had to implemented all EU legislation 158. Does your inspection strategy consider the enforcement strategy developed by the FORUM and the activities carried out there? Forum strategy as described in the document Strategies for enforcement of Regulation (EC). 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC). 1272/2008 on the classification, labelling and packaging of substances and mixtures (CLP) as adopted at the 9th meeting of the Forum on 1-3 March Please provide examples: 159. Please provide the total number of inspectors that attended training on REACH in your Member States in the reporting period ( )? 50 Co-ordination, co-operation and exchange of information Explanation of the co-ordination, co-operation and exchange of information, between enforcing authorities, with Competent Authorities and other authorities from other Member States 27

28 160. Please outline the mechanisms/procedures put in place to ensure cooperation, coordination and exchange of information on REACH enforcement between enforcing authorities and other authorities (within or outside your Member State): In national law procedures are included Describe how these mechanisms have operated in practice during the reporting period (e.g. regular meetings, joint training, joint inspections, co-ordinated projects and so on): we have joint inspecitons 162. From Forum activities, which ones do you consider most relevant to enhance coordination, cooperation and exchange of information among Member States: ref projects Please provide examples: 28

29 163. Provide details on enforcement activities carried out with other Member States outside the remit of the Forum: we didn't have it 164. Describe any other measures/relevant information: For a definition of 'measure', please refer to the glossary Reporting on enforcement activities dutyholders 165. Provide an estimate of the total number of dutyholders who are likely to have duties imposed on them by REACH: For a definition of 'dutyholder' please refer to the glossary. The dutyholder principal role is the highest position the dutyholder has within the supply chain. For example, if a manufacturer of a substance is also a downstream user of others, then its principal role should be regarded as manufacturer. If no information is available for a specific year, please indicate N/A in the corresponding box dutyholders N/A N/A N/A

30 166. Provide an estimate of the above dutyholders who are likely to be considered as registrants as defined by REACH: If no information is available for a specific year, please indicate N/A in the corresponding box dutyholders N/A N/A N/A What was the total number of official controls such as inspections or investigations or monitoring, or other enforcement measures carried out by enforcing authorities in which REACH was covered and/or enforced during the reporting period? For definitions of 'investigation' or 'monitoring', please refer to the glossary State the number of manufacturers subject to enforcement activities: If no information is available for a specific year, please indicate N/A in the corresponding box manufacturers N/A N/A N/A Were these mainly: For definitions of micro, small and medium-sized enterprises, please refer to the glossary. The category 'not applicable' can be filled in case you have information on the size of industry but it does not allow you to complete the three categories (Small, Medium, Large). Micro Small Medium Large information N/a

31 169. State the number of only representatives subject to enforcement activities: If no information is available for a specific year, please indicate N/A in the corresponding box only representatives N/A N/A N/A N/A N/A Were these mainly: Micro Small Medium Large information N/a State the number of distributors subject to enforcement activities: If no information is available for a specific year, please indicate N/A in the corresponding box distributors N/A N/A N/A Were these mainly: Micro Small Medium Large information N/a

32 171. State the number of downstream users subject to enforcement activities: If no information is available for a specific year, please indicate N/A in the corresponding box downstream users N/A N/A N/A Were these mainly: Micro Small Medium Large information N/a State the number of importers subject to enforcement activities: importers N/A N/A N/A Were these mainly: Micro Small Medium Large information N/a

33 official controls prompted by 173. Have there been complaints or concerns received by enforcing authorities in relation to alleged contraventions of the REACH Regulation? Controls are understood as inspections or investigations or monitoring, or other enforcement measures carried out by enforcing activities controls N/A N/A N/A N/A N/A 174. Incidents (e.g. accidents such as poisoning or other dangerous occurrences)? controls N/A N/A N/A N/A N/A 175. Monitoring activities? controls N/A N/A N/A N/A N/A 176. Results of an inspection? controls N/A N/A N/A official controls which addressed 33

34 177. Registration: Controls are understood as inspections or investigations or monitoring, or other enforcement measures carried out by enforcing activities controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 178. Registration and notification of substances in Articles: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 179. Information in the supply chain: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 180. Duty to communicate information on substances in articles: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 34

35 181. Restrictions: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 182. Authorisations: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A 183. Imported goods: controls N/A N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A N/A official controls which resulted in areas of infringement found: controls N/A N/A N/A N/A N/A 35

36 185. Verbal or written advice: controls N/A N/A N/A Legal proceedings: controls N/A N/A N/A Convictions: controls N/A N/A N/A Other: controls N/A N/A N/A N/A N/A If 'Other', please specify: 189. Please provide information on difficulties encountered during REACH official controls: 36

37 190. Please provide information on good practices related to REACH official controls: Sanctions 191. Describe the different sanctions that can be used in case of contravention of REACH, e.g. enforcement notices and other sanctions such as on-the-spot fines or undertakings, official reprimands such as formal cautions or warnings, and legal proceedings (whether criminal or civil in nature): The answer to this question is to be given only if the position has changed since the last reporting period. Appeals 192. Please state the number of appeals against REACH enforcement National Enforcement Authority decisions in your Member State in the reporting period ( ): 193. Please state the number of REACH enforcement National Enforcement Authority decisions in your Member State that were overturned by ruling of a domestic or EU court of law in the reporting period ( ): Theme 10: CLP enforcement activities General information 37

38 194. Please explain how competent authorities are organised for the enforcement of CLP in your country; please concentrate on the changes from the last reporting: Ministry of Health is NEA 195. How many authorities are in charge of CLP enforcement? Please provide their names: Describe the general status of the resources allocated to enforcing authorities for tasks related to the enforcement of CLP (assessment of annual budget and staff): 4 inspectors in national level 20 inspectors in regional level Enforcement Strategy(ies) General information on the enforcement strategy (or strategies) in place within the Member State 197 Has an overall strategy or strategies been implemented for the enforcement of the CLP Regulation? 38

39 198. Is(are) the strategy(ies) in line with the strategy devised by the Forum? Forum strategy as described in the document Strategies for enforcement of Regulation (EC). 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC). 1272/2008 on the classification, labelling and packaging of substances and mixtures (CLP) as adopted at the 9th meeting of the Forum on 1-3 March Please outline the enforcement strategy within the Member State, and the methodology/techniques used (this should include a description of the criteria by which dutyholders were selected for enforcement activities): Strategy is incorporated in national laws 200. Provide information on the level and extent of monitoring activities undertaken (this should include a description of the criteria by which substances, mixtures, articles etc. were selected for monitoring): For a definition of monitoring activities, please refer to the glossary. according to the annually programm 201. Is this enforcement strategy publicly available? Inspection Strategy 39

40 203. Describe the CLP inspection strategy: For a definition of 'inspection', please refer to the glossary How has the inspection strategy evolved from 2011 to 2014? Since July 2013 we started to implement eu legislation 205. Does your inspection strategy consider the enforcement strategy developed by the FORUM and the activities carried out there? Forum strategy as described in the document Strategies for enforcement of Regulation (EC). 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC). 1272/2008 on the classification, labelling and packaging of substances and mixtures (CLP) as adopted at the 9th meeting of the Forum on 1-3 March Please provide examples: 206. Please provide the total number of inspectors that attended training on CLP in your Member State in the reporting period ( ): 20 Co-ordination, co-operation and exchange of information 40

41 Explanation of the co-ordination, co-operation and exchange of information, between enforcing authorities, with Competent Authorities and other authorities from other Member States 207. Please outline the mechanisms/procedures put in place to ensure cooperation, coordination and exchange of information on CLP enforcement between enforcing authorities and other authorities (within or outside your Member State): Mechanisms and procedures are put in national legislation (law and sublaws) 208. Describe how these mechanisms have operated in practice during the reporting period (e.g. regular meetings, joint training, joint inspections, co-ordinated projects and so on): joint inpsections, co-ordinated projects Reporting on enforcement activities 209. What was the total number of official controls, such as inspections or investigations, or other enforcement measures carried out by enforcing authorities in which CLP was covered and/or enforced during the reporting period? For a definition of 'inspection' and 'investigation', please refer to the glossary controls N/A N/A multipaging 41

42 210. If applicable, please add a description of the other enforcement measures carried out in this reporting period: dutyholders 211. Provide an estimate of the total number of dutyholders who are likely to have duties imposed on them by CLP: For a definition of 'dutyholder', please refer to the glossary. The dutyholder principal role is the highest position the dutyholder has within the supply chain. For example, if a manufacturer of a substance is also a downstream user of others, then its principal role should be regarded as manufacturer dutyholders Dutyholders subject to official controls 212. State the number of manufacturers subject to enforcement activities under CLP: manufacturers N/A N/A

43 Were these mainly: For definitions of micro, small and medium-sized enterprises, please refer to the glossary. The category not applicable can be filled in case you have information on the size of industry but it does not allow you to complete the three categories (Small, Medium, Large). Micro Small Medium Large information N/a State the number of distributors subject to enforcement activities under CLP: distributors N/A N/A Were these mainly: Micro Small Medium Large information N/a State the number of downstream users subject to enforcement activities under CLP: downstream users N/A N/A

44 Were these mainly: Micro Small Medium Large information N/a State the number of importers subject to enforcement activities under CLP: importers N/A N/A Were these mainly: Micro Small Medium Large information N/a official controls prompted by 44

45 216. Have there been complaints or concerns received by enforcing authorities in relation to alleged contraventions of the CLP Regulation? Controls are understood as inspections or investigations or monitoring, or other enforcement measures carried out by enforcing activities controls N/A N/A Incidents (e.g. accidents such as poisoning or other dangerous occurrences)? controls N/A N/A Monitoring activities? controls N/A N/A Results of an inspection? controls N/A N/A N/A N/A official controls which addressed 220. Hazard classification: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 45

46 221. Hazard communication in the form of labelling: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 222. Packaging: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 223. Harmonisation of classification and labelling of substances: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 224. tification to the classification and labelling inventory according to Article 40: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 46

47 225. Other common provisions, such as the obligation to maintain information and requests for information: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 226. Imported goods: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A 227. Other CLP obligations: controls N/A N/A N/A N/A Cases of non-compliance found N/A N/A N/A N/A official contols which resulted in areas of infringement found: controls N/A N/A N/A N/A 229. Verbal or written advice: controls N/A N/A

48 230. Legal proceedings: controls N/A N/A Convictions: controls N/A N/A Other: controls N/A N/A 0 0 If 'Other', please specify: Sanctions 233. Describe the different sanctions that can be used in case of contravention of the CLP Regulation, e.g. enforcement notices and other sanctions such as on-the-spot fines or undertakings, official reprimands such as formal cautions or warnings, and legal proceedings (whether criminal or civil in nature): The answer to this question needs only be given if the position has changed since the last reporting period or is different to that provided by virtue of CLP Article

49 Appeals 234. Please state the number of appeals against CLP enforcement National Enforcement Authority decisions in your Member State in the reporting period ( ): 235. Please state the number of CLP enforcement National Enforcement Authority decisions in your Member State that were overturned by ruling of a domestic or EU court of lawnew Number Question in the reporting period ( ): Other enforcement activity not covered elsewhere 236. Provide details on enforcement activities carried out at the request / suggestion of ECHA: 237. Provide details on enforcement activities carried out at the request of other Member States, e.g. where cross-border issues are detected and communicated: 238. Detail any other measures taken pursuant to articles 46(1) and 47 of the CLP Regulation, or any other information you wish to provide for the purposes of this part of the Report: For a definition of 'measure', please refer to the glossary. 49

50 Theme 11: Information on the effectiveness of REACH on the protection of human health and the environment, and the promotion of alternative methods, and innovation and competition 239. Do you think that the effects of REACH would be better evaluated at a Member State or at EU level? Member State level EU level 240. Please provide a brief explanation of your response: 241. What parameters are available at Member State level that could be used to assess the effectiveness of REACH in a baseline study? Theme 12: Other issues / recommendations / ideas 242. Please provide any further information on the implementation of REACH that the Member State considers relevant: 2500 character(s) maximum 50

51 243. Do you wish to upload documents in support of this submission? You may upload one or more documents. Background Documents Glossary (/eusurvey/files/457b4be8-39e0-4dc4-87ba ec1ddb) Contact 51