MINIMUM CRITERIA FOR REACH AND CLP INSPECTIONS 1
|
|
- Lisa Young
- 5 years ago
- Views:
Transcription
1 FORUM FOR EXCHANGE OF INFORMATION ON ENFORCEMENT Adopted at the 9 th meeting of the Forum on 1-3 March 2011 MINIMUM CRITERIA FOR REACH AND CLP INSPECTIONS 1 MARCH First edition adopted at the 6 th meeting of the Forum on 8-10 December 2009
2 Contents Introduction Purpose Definitions Scope and general principles Enforcement strategies Organisation Planning Carrying out REACH and/or CLP inspection 9 8. Action following REACH and/or CLP inspection Checking and review of national arrangements Reporting Review of the minimum criteria Introduction (i) (ii) (iii) (iv) Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) entered into force on 1 June It introduced a new system for controlling chemicals across the EU., Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 concerning the classification, labelling and packaging of substances and mixtures (CLP) entered into force on 20 January The CLP Regulation made amendments to Regulation (EC) No 1907/2006 and will repeal the Directives 67/548/EEC and 1999/45/EC on 1 June 2015,. In order to enable the system introduced by REACH and CLP to operate effectively in practice, Member States are obliged to establish the necessary arrangements for its implementation and enforcement. One of the most important elements of the overall enforcement of both Regulations is inspection. Recital 121 of REACH and recital 59 of CLP states that Member States should put in place effective monitoring and control measures. Article 125 of REACH and Article 46 of CLP requires Member States to maintain a system of official controls and other activities as appropriate to the circumstances, and Article 126 of REACH and Article 47 of CLP requires Member States to lay down the provisions on penalties applicable for infringement of REACH or CLP which must be effective, proportionate and dissuasive. Under Articles 117(1) and 127 of REACH, the results of inspections, monitoring, penalties and other measures are to be reported to the European Commission by 1 June 2010 and after that every five years. Article 46(2) of CLP states that the Member States shall submit a report to the Agency (ECHA) every five years (by the 1 July) on the results of the official controls and other enforcement measures taken. Recital 120 of REACH and recital 61 of CLP also recognise the need for good cooperation, coordination and exchange of information between the Member States, the European Chemicals Agency (ECHA) and the European Commission. REACH establishes, in Article 76, a Forum for Exchange of Information on Enforcement ( the Forum ), which is allocated certain tasks such 1
3 as coordinating harmonised enforcement projects, identifying enforcement strategies and best practice in enforcement, developing working methods and tools for inspectors, and developing an electronic information exchange procedure. Article 46(3) of CLP states that this Forum also shall undertake those tasks in respect of the enforcement of CLP. (v) (vi) (vii) (viii) (ix) Different systems and practices of inspection exist in Member States and this document does not propose that they be replaced by a system of inspection at EU level. Member States should retain responsibility for REACH and CLP inspection activities. Instead, the purpose of this document is to establish guidelines, in the form of minimum criteria, to be applied as a common basis for the performance of REACH and CLP inspection activities within the Member States and EEA-EFTA States. This is consistent with some of the principle tasks of the Forum under Articles 76(1)(f) and 77(4) of REACH to coordinate a network of Member States authorities responsible for the enforcement of REACH, and to identify best practice in enforcement. The Forum is also responsible for coordinating a network of authorities responsible for the enforcement of CLP according to Article 46(3) of CLP. The Forum has, since its establishment, mandated a number of Working Groups to carry forward various elements of its work programme. References are made to the work of existing Forum Working Groups where appropriate and, in particular, the Forum document Strategies for enforcement of Regulation (EC) no. 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC) no. 1272/2008 on the classification, labelling and packaging of substances and mixtures (CLP) as adopted in March 2009 by the Forum and subsequently revised. The minimum criteria for REACH and CLP inspections elaborated in this document have been created to be consistent with the output of other Forum Working Groups and, in particular, are intended to operate alongside the enforcement strategies document on an equal footing. Minimum criteria have already been set for environmental inspections under the Recommendation no. 2001/331/EC of the European Parliament and the Council of 4 April 2001 providing for minimum criteria for environmental inspections (RMCEI), as elaborated by the European Union Network for the Implementation and Enforcement of Environmental Law (IMPEL) and already adopted by the majority of the Member States. Although not directly applicable to REACH and CLP, the RMCEI provides a useful foundation upon which a structured system for REACH and CLP inspections can be created. REACH and CLP fall within the scope of Regulation (EC) No 765/2008 of the European Parliament and of the Council setting out the requirements for accreditation and market surveillance ( the AMS Regulation ), insofar as there are no specific provisions with the same objective, nature or effect in REACH or CLP. Member States must therefore ensure that REACH and CLP are included within their overall provisions for the implementation of the AMS Regulation. To this effect, this document is designed to incorporate, and be consistent with, the relevant requirements of the AMS Regulation. Implementation of the minimum criteria for REACH and CLP inspections should therefore achieve the relevant requirements of the AMS Regulation (insofar as these can be met without further legislation being required within the Member State). When considering REACH and CLP in the context of the 2
4 AMS Regulation, Member States should ensure that equal prominence is given to both environmental protection and human health. (x) The Forum mandated a Working Group in December 2008 to develop minimum criteria for REACH inspections, in order to ensure the level playing field within the internal market and the better co-ordination of REACH enforcement within Member States and EEA-EFTA States. In May 2010 the Forum mandated a Working Group to update these minimum criteria so that they covered also CLP inspections among other things. This document represents the output of these Working Groups, as ultimately adopted by the Forum. 1. Purpose 1. REACH and CLP inspection activities should be carried out in Member States following minimum criteria to be applied in the effective organisation, planning, implementation, carrying out and review of such tasks, thereby strengthening duty holder compliance with REACH and CLP, as well as contributing to more harmonised enforcement. These are key factors in realising the objectives of REACH and CLP to ensure a high level of protection of human health and the environment as well as the free movement of substances while enhancing competitiveness and innovation. 2. This document is addressed to enforcing authorities (and other public authorities as appropriate) in Member States with responsibilities for the matters contained within this document. 1. In this document 2. Definitions a) REACH means Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (OJ L 396, , p1) as amended. b) CLP means Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 concerning the classification, labelling and packaging of substances and mixtures (OJ L 353, , p1) as amended. c) the AMS Regulation means Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance (OJ L 218, , p30). d) REACH and CLP inspections means the range of activities an enforcing authority may undertake in order to assess, secure or promote a dutyholder s compliance with REACH and/or CLP. Such activities may be routine (proactive) or non-routine (reactive), and include inspection, investigation, monitoring, formal enforcement and other measures taken in pursuance of 3
5 Articles 125 and 126 of REACH and of Articles 46 and 47 of CLP, as defined in the following sub-paragraphs: (i) (ii) (iii) (iv) inspection refers to a proactive (planned and routine) process that involves collecting information to make an assessment of a dutyholder s current level of compliance, by comparing their activities to the legal requirements and benchmark standards relevant to the activities in question. Information may be obtained by reviewing relevant documents held by the dutyholder or available to the enforcing authority, and/or interviewing people, and/or monitoring, and/or observing site conditions, standards or practices where activities subject to the requirements of REACH and CLP are carried out under the dutyholder's control. It follows that REACH and CLP inspection activity can occur at or away from a dutyholder s premises. investigation refers to a reactive (non-routine) process which includes all those activities carried out in response to an accident, incident, complaint, referral from another enforcing authority or public body, or an identified non-compliance, to gather and establish the facts, detect contraventions of REACH or CLP duties, identify immediate and underlying causes and the lessons to be learned, prevent recurrence, and take appropriate action, including formal enforcement. monitoring means periodic or continuous surveillance, measurement, sampling, testing and/or analysis of various media, such as substances, mixtures, articles, the environment (air, water, soil, vegetation, animals) and so on, to determine the level of compliance with statutory requirements. formal enforcement refers to a range of enforcement activity an enforcing authority is statutorily empowered to take, such as bringing legal proceedings by criminal or civil means, serving enforcement notices or other such administrative penalties (such as undertakings or on-the-spot fines), issuing formal cautions, and so on. e) enforcing authority means any public authority at national, regional or local level, which is established or designated by the Member State and is responsible for enforcement of the matters that are covered by this document. f) the Forum means the Forum for Exchange of Information on Enforcement, as established by Article 76(1)(f) of REACH. g) dutyholder means any person (whether natural or legal) with obligations under REACH or CLP, other than enforcing authorities, Competent Authorities, the European Chemicals Agency (ECHA) or the European Commission. h) target group means a group of dutyholders who exercise a particular activity and have a characteristic set of obligations according to REACH or the CLP. Regulations. Target groups under REACH and/or CLP are manufacturers, importers, distributors, only representatives (under REACH) and downstream users of substances, mixtures or articles. i) risk analysis means the determination of the impact and the probability of non-compliance with REACH and/or CLP requirements in order to consider 4
6 how this should influence the priorities of enforcing authorities. Impacts include environmental, occupational health and safety, public health, consumer protection and economic effects. Probability could be assumed as a function of the level of awareness and knowledge and the level of acceptance of REACH and CLP by the target groups, combined with their estimation of the economic implications of complying with REACH and/or CLP, the probability of being found in non-compliance, the probability of sanctions being imposed by enforcing authorities, and the possibility of adverse public reaction. j) risk assessment is the estimation of the acceptability of the risk determined by the risk analysis. If the risk is unacceptable, preventive or correction measures have to be applied. k) product shall have the meaning assigned to it under Article 15(4) of the AMS Regulation. l) market surveillance shall mean the activities carried out and measures taken by enforcing authorities according to chapter III of the AMS Regulation. 2. All references to Member States in this document should be read as including EEA-EFTA States unless otherwise provided. 3. Other expressions used in this document which are used in REACH or CLP have the same meaning that they bear in REACH or CLP. 3. Scope and general principles 1. This document applies to all REACH and CLP inspection activities undertaken by the enforcing authorities of Member States that are intended to address issues of compliance with REACH and CLP by all dutyholders whose activities are subject to its requirements. 2. In determining how best to implement the minimum criteria for REACH and CLP inspections as set out in this document, enforcing authorities should have regard to the following general principles: a) REACH and CLP should be effectively enforced, but in ways which minimise the burden of checking compliance for both dutyholders and for enforcing authorities. b) Comprehensive risk analysis should be used to ensure that enforcing authorities concentrate their resources on the areas that need them the most. Risk analysis in this context should follow the principles laid down in the document Strategies for enforcement of Regulation (EC) no. 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC) No 1272/2008 ot the European Parliament and of the Council of 16 December 2008 concerning the classification, labelling and packaging of substances and mixtures as adopted by the Forum. In particular, risk analysis should be based on all available relevant and good-quality data. 5
7 c) Enforcing authorities should respond proportionately to identify contraventions of REACH or CLP, and within the framework of their enforcement policies, in order to deliver desirable regulatory outcomes. In particular, enforcing authorities should ensure that products which present a serious risk requiring rapid intervention, including a serious risk where the effects are not immediate, are treated in accordance with the requirements of Articles 20 and 29 of the AMS Regulation (inter alia, recalling, withdrawing or destroying such products or prohibiting them from being made available on the market). d) Dutyholders should be helped and encouraged to understand and meet their obligations under REACH and CLP more easily. This includes the provision of readily accessible advice and guidance. e) Enforcing authorities shall carry out their duties independently, impartially and without bias. 4. Enforcement strategies In order to be able to have a structured and transparent approach to REACH and CLP enforcement, an appropriate enforcement strategy or strategies should be developed. The strategy or strategies should use the general framework as described in the document Strategies for enforcement of Regulation (EC) no. 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) and of Regulation (EC) no. 1272/2008 of the European Parliament and of the Council of 16 December 2008 concerning the classification, labelling and packaging of substances and mixtures as adopted by the Forum.. 5. Organisation 1. Appropriate provisions should be made to ensure, as far as is reasonably practicable, that enforcing authorities cooperate and exchange information (as mentioned in Article 122 of REACH and Article 43 (2) of CLP) with: a) other enforcing authorities within their Member State; b) their Competent Authority or Authorities; c) enforcing authorities or Competent Authorities in other Member States; and d) the European Chemicals Agency; where this will facilitate compliance with, or the effective enforcement of REACH and CLP (with reference to the requirements of the AMS Regulation, insofar as there are no specific provisions with the same objective, nature or effect in REACH or CLP) in the Member States. 2. Where not already provided for by national law, formal arrangements should be devised and implemented as appropriate that provide for clear and effective cooperation and information exchange between enforcing authorities within a Member State (where there is more than one enforcing authority responsible for the enforcement of REACH and CLP). Such arrangements should contain provisions as to: 6
8 a) joint working should enforcement responsibilities overlap; b) the sharing of information between enforcing authorities regarding their REACH and CLP inspection activities and issues giving rise to concern, and the manner in which this is to be achieved. The electronic information exchange system adopted by the Forum for the purposes of REACH and CLP enforcement should be used for fast and easy exchange of information; c) co-operation and information exchange with customs authorities (where customs authorities are not already a designated REACH and/or CLP enforcing authority within a Member State); d) notification between enforcing authorities of identified matters of concern regarding dutyholders; e) supporting each other with enforcement, and where appropriate the provision of specialist advice; and f) if appropriate, the establishment of national, regional and/or local networks or fora for enforcement liaison. 3. Information about the enforcing authorities, their tasks and responsibilities and how they may be contacted should be publicly available in all Member States. 4. Matters of concern identified through REACH and/or CLP inspection activity that relate to the compliance of dutyholders based in other Member States, or that appear to raise significant cross-border issues, should be communicated as soon as possible via the electronic information exchange system adopted by the Forum for the purposes of REACH and CLP enforcement. Information on general enforcement issues with Community-wide interest should be exchanged via the Forum. 5. Enforcing authorities should disclose to the bodies referred to in paragraph (1) information they hold in relation to compliance with, or the enforcement of, REACH and/or CLP where they believe: a) it is reasonable to make that disclosure; b) such disclosure is lawfully allowed by national legislation; and c) the disclosure will facilitate compliance with, or the effective enforcement of, REACH and CLP in Member States. 6. Enforcing authorities should ensure that they make appropriate resources available for REACH and CLP inspection, and that inspectors (and other relevant staff as may be necessary) have suitable qualifications and have been given the necessary powers to enforce those parts of REACH and/or CLP for which they have enforcement responsibility. Suitable training and up to date support materials should be provided to those involved in REACH and/or CLP inspection. 6. Planning 1. Enforcing authorities should ensure that their REACH and CLP inspection activities are planned in advance, by having at all times an inspection plan or plans, 7
9 collectively taking into account all the territory of the Member State and of the known target groups. 2. Such plan or plans may be established at national, regional or local levels, but enforcing authorities should ensure that the plan or plans apply to all of their REACH and CLP inspections and that the plans have regard to the strategy or strategies developed in accordance with section 4 above. 3. Plans for REACH and CLP inspection should be produced on the basis of the following: a) the enforcing authorities objectives and targets, their overall statutory responsibilities and competencies, and the provisions of REACH and/or CLP they are responsible for enforcing; b) the known dutyholders / target groups within the area(s) covered by the plan; c) the resources available to the enforcing authorities; d) a general analysis of major public, occupational health and environmental risks within the area(s) covered by the plan, taking into account the hazards arising from the activities of the dutyholders / target groups, the likelihood of the hazards occurring, and the vulnerability of those who could be affected by those activities (workers, the general public, the environment); e) a general appraisal of the likelihood of non-compliance by the dutyholders / target groups with REACH and/or CLP requirements, taking into account factors such as previous inspection records and potential future risks. 4. Plans for REACH and CLP inspection should: a) be appropriate to the inspection tasks / competencies of the relevant enforcing authorities; b) take into account the number and size of the different dutyholders / target groups concerned; c) take into account relevant existing information in relation to specific dutyholders, such as safety data sheets, chemical safety reports, information used for the purposes of classification and labelling, other information available from the electronic information exchange system (as adopted by the Forum) or from REACH-IT or RIPE, results of previous inspections, or information kept and made available by the dutyholders according to Article 36 of REACH or Article 49 of CLP; d) consider the amount and suitability of existing information available to the enforcing authority, and the need for further work to better identify dutyholders / target groups and gather intelligence on supply chain information, so as to provide for more effective risk analysis, and targeting and use of resource; and e) give priority to measures that are designed to achieve an effective outcome in terms of compliance, based on risk analysis. 5. Each plan for REACH and/or CLP inspection should, as a minimum: 8
10 a) define the geographical area which it covers, which may be for all or part of the territory of a Member State; b) cover a defined time period, for example one year; c) provide for co-ordination, co-operation, communication and information exchange in accordance with section 5 above; d) provide for routine (proactive) REACH and/or CLP inspection, which identifies the specific dutyholders / target groups covered and which describes the scope and, if possible, the frequency of the inspection; e) provide and outline the procedures for non-routine (reactive) REACH and/or CLP inspection, ensuring that appropriate resources can be set aside as necessary; and f) include specific provisions for its revision. 7. Carrying out REACH and/or CLP inspection Enforcing authorities should apply the following criteria in respect of all REACH and/or CLP inspection: a) that the role of the dutyholder is correctly identified (in terms of which of the target groups they belong to); b) that an appropriate check is made of compliance with the REACH and/or CLP requirements relevant to the particular scope of the inspection and according to the role of the dutyholder (i.e. to the different obligations of the target groups registration, information in the supply chain, use, authorisation, restriction, classification, labelling, notification or other REACH or CLP duties as appropriate); c) that if site visits are to be carried out by more than one enforcing authority, then as far as possible they exchange information on each others' activities and co-ordinate site visits and other REACH and/or CLP inspection work; d) that the findings of the inspections are contained in reports which contain the information needed by the Member State for the purposes of reporting under Article 117(1) of REACH (with reference to Article 127) and under Article 46 of CLP. Such reports should be exchanged as necessary between relevant enforcing authorities, Competent Authorities and other bodies, on an international, national, regional or local level by using the electronic information exchange system (as adopted by the Forum); e) the essential requirements of REACH and CLP, as prioritised in the national REACH and CLP enforcement strategies, relevant for the given dutyholder / target group are examined, in accordance with REACH and CLP requirements, the inspection plan(s) and the enforcing authorities responsibilities and competencies; f) that the inspections promote dutyholders' knowledge and understanding of their duties under REACH and CLP, and ensure dutyholder compliance (using formal enforcement where appropriate); 9
11 g) that the risks to, and impact on, human health and the environment are considered; h) that complaints received by enforcing authorities and made by third parties, who make allegations relating to the compliance of a particular dutyholder or dutyholders, are investigated as soon as possible after such complaints are received, in line with any relevant selection criteria that enforcing authorities may apply; i) that serious accidents or incidents are investigated without undue delay after these come to the notice of the relevant enforcing authorities, in line with any relevant accident or incident selection criteria they may apply; j) that products identified during REACH and/or CLP inspection activities which present a serious risk requiring rapid intervention, including a serious risk where the effects are not immediate, are treated in accordance with the requirements of Articles 20 and 29 of the AMS Regulation; k) that, if hazards are identified related to any product, the enforcing authorities shall take measures to alert users by using the appropriate procedures as required by Article 19(2) of the AMS Regulation; l) that recall or withdrawal of products, or prohibitions on making products available on the market, has to be carried out according to the provisions of Articles 19 to 29 of the AMS Regulation; and m) that enforcing authorities preserve confidentiality where necessary in order to protect commercial secrets or to preserve personal data pursuant to national legislation, although this shall not prevent the dissemination of relevant information to relevant enforcing authorities and to the public as necessary, in order to protect the interests of users in the Community. 8. Action following REACH and/or CLP inspection 1. Enforcing authorities should ensure that after every inspection without unnecessary delay relevant inspection reports are produced and stored, which as a minimum contain: a) basic data on the inspection (for example, the date, name of the inspector(s), scope of the inspection, details of the dutyholder etc); b) the significant findings of the REACH and/or CLP inspection; c) a comparison of the findings with the legal requirements, relevant to the dutyholder / target group concerned; d) an evaluation thereof, identification of any non-compliance, and a conclusion on whether any further action should follow, such as formal enforcement or further inspections; and e) the measures taken pursuant to the REACH and/or CLP inspection, by the enforcing authority and/or by the dutyholder. 10
12 2. The inspection reports should be properly recorded in writing and kept in an accessible and retrievable format. The reports should be communicated to dutyholders promptly with clear explanations of what action they are required to take. 3. The enforcing authorities should ensure that if a dutyholder is required to take action in response to an inspection, then appropriate checks are made where necessary to ascertain that the required action has been taken, and as soon as possible after the expiry of any deadline given to the dutyholder. The failure of the dutyholder to complete the activities required should result in further enforcement action to ensure compliance. 9. Checking and review of arrangements for REACH and/or CLP inspection Enforcing authorities should regularly check and review the success of their arrangements for REACH and CLP inspections, including the elements of organisation, planning and carrying out, using appropriate performance indicators. If necessary, the arrangements should be updated in order to further the effectiveness of REACH and CLP inspections. 10. Reporting Enforcing authorities should ensure that appropriate systems are in place to facilitate the collection and collation of relevant information on REACH and CLP inspection activities. For these purposes, relevant information means as a minimum the enforcement-related information that is required to be submitted to the European Commission for the purposes of reporting under Article 117(1) of REACH (with reference to Article 127) and under Article 46 of CLP, and as elaborated by the Forum through its Working Group on the Member States Report to the Commission. 11. Review of the minimum criteria 1. The Forum should review the operation and effectiveness of this document no later than the end of December 2010 and thereafter at least once every five years, with the intention of developing the minimum criteria further in terms of their scope and application. This will be undertaken in the light of the experience gained from their application, and taking into account any contributions from interested parties, including Member States, the European Commission and the European Chemicals Agency. 2. The Forum may review this document more frequently than the minimum timescales set out above if it so chooses. The review may also include a review of all, or a selection of, the approaches of Member States to implementing the minimum criteria, in order to identify and spread best practice for REACH and CLP enforcement, in line with the requirements of Article 77(4) of REACH. 11
FORUM FOR EXCHANGE OF INFORMATION ON ENFORCEMENT. Disclaimer:
FORUM FOR EXCHANGE OF INFORMATION ON ENFORCEMENT Adopted at the 9 th meeting of the Forum on 1-3 March 2011 Strategies for enforcement of Regulation (EC) no. 1907/2006 concerning the Registration, Evaluation,
More informationCHEMICALS (Classification, Labelling, Packaging of substances and mixtures -CLP) Screening Meeting EU Serbia June 2013
CHEMICALS (Classification, Labelling, Packaging of substances and mixtures -CLP) Screening Meeting EU Serbia June 2013 Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances
More informationOfficial Journal of the European Union
L 33/30 DIRECTIVE 2002/98/EC OF THE EUROPEAN PARLIAMT AND OF THE COUNCIL of 27 January 2003 setting standards of quality and safety for the collection, testing, processing, storage and distribution of
More informationAdopted by Pharmacovigilance Risk Assessment Committee 20 February Adopted by Pharmacovigilance Inspectors Working Group 21 March 2014
21 March 2014 EMA/INS/PhV/192231/2014 Union procedure on the management of pharmacovigilance inspection findings which may impact the robustness of the benefit-risk profile of the concerned medicinal Adopted
More informationCOMMISSION IMPLEMENTING REGULATION (EU)
L 253/8 Official Journal of the European Union 25.9.2013 COMMISSION IMPLEMENTING REGULATION (EU) No 920/2013 of 24 September 2013 on the designation and the supervision of notified bodies under Council
More informationREPUBLIC OF SERBIA Bilateral screening: Chapter 1 Free Movement of Goods. C L P Classification, Labeling and Packaging of substances and mixtures
REPUBLIC OF SERBIA Bilateral screening: C L P Classification, Labeling and Packaging of substances and mixtures C O N T E N T STATE OF PLAY LEGISLATIVE FRAMEWORK COMPETENT AUTHORITY (CA) ADMINISTRATIVE
More informationBilateral screening: Chapter 27 PRESENTATION OF THE REPUBLIC OF SERBIA Classification, labelling and packaging of substances and mixtures - CLP
REPUBLIC OF SERBIA Negotiating Group for the Chapter 27 Environment and Climate Change Bilateral screening: Chapter 27 PRESENTATION OF THE REPUBLIC OF SERBIA Classification, labelling and packaging of
More informationRECOMMENDATIONS ON CLOUD OUTSOURCING EBA/REC/2017/03 28/03/2018. Recommendations. on outsourcing to cloud service providers
EBA/REC/2017/03 28/03/2018 Recommendations on outsourcing to cloud service providers 1. Compliance and reporting obligations Status of these recommendations 1. This document contains recommendations issued
More informationRecommendations on outsourcing to cloud service providers (EBA/REC/2017/03)
Recommendations on outsourcing to cloud service providers (EBA/REC/2017/03) These Recommendations of the European Banking Authority (EBA) are addressed to competent authorities as defined in point (i)
More informationBrussels, 12 June 2014 COUNCIL OF THE EUROPEAN UNION 10855/14. Interinstitutional File: 2012/0266 (COD) 2012/0267 (COD)
COUNCIL OF THE EUROPEAN UNION Brussels, 12 June 2014 Interinstitutional File: 2012/0266 (COD) 2012/0267 (COD) 10855/14 PHARM 44 SAN 232 MI 492 COMPET 405 CODEC 1471 NOTE from: General Secretariat of the
More informationSAFETY, HEALTH AND WELLBEING POLICY
LEEDS BECKETT UNIVERSITY SAFETY, HEALTH AND WELLBEING POLICY www.leedsbeckett.ac.uk/staff Policy Statement The University is committed to provide a safe and healthy environment for work and study in support
More informationFood Standards Agency in Wales
Food Standards Agency in Wales Report on the Focused Audit of Local Authority Assessment of Regulation (EC) No 852/2004 on the Hygiene of Foodstuffs in Food Business Establishments Torfaen County Borough
More informationCOMMISSION IMPLEMENTING DECISION. of
EUROPEAN COMMISSION Brussels, 16.10.2014 C(2014) 7489 final COMMISSION IMPLEMENTING DECISION of 16.10.2014 laying down rules for the implementation of Decision No 1313/2013/EU of the European Parliament
More informationHealth and Safety Policy
Health and Safety Policy 2015 Statement of Health and Safety Policy The University recognises its obligations to properly control the risks to the health of its staff, students and visitors. Strong strategic
More informationGuideline on good pharmacovigilance practices (GVP)
1 2 26 July 2012 EMA/118465/2012 3 4 Guideline on good pharmacovigilance practices (GVP) Module XV Safety communication 5 Draft finalised by the Agency in collaboration with Member States and submitted
More informationASSESSMENT OF THE CONSOLIDATED ANNUAL ACTIVITY REPORT OF THE AUTHORISING OFFICER FOR THE YEAR 2014
Management Board Decision 07/2015 1(5) ASSESSMENT OF THE CONSOLIDATED ANNUAL ACTIVITY REPORT OF THE AUTHORISING OFFICER FOR THE YEAR 2014 THE MANAGEMENT BOARD, Having regard to Regulation (EC) No 1907/2006
More informationMEDICINES FOR HUMAN USE (CLINICAL TRIALS) REGULATIONS Memorandum of understanding between MHRA, COREC and GTAC
MEDICINES FOR HUMAN USE (CLINICAL TRIALS) REGULATIONS 2004 Memorandum of understanding between MHRA, COREC and GTAC 1. Purpose and scope 1.1 Regulation 27A of the Medicines for Human Use (Clinical Trials)
More informationECHA and the implementation of REACH,CLP and other tasks
ECHA and the implementation of REACH,CLP and other tasks Eva Sandberg International Unit www.kemi.se ECHA, its tasks and organisation European Chemicals Agency ECHA REACH Regulation entered into force
More informationSt Anne's Community Services Staff Manual
4.01 St Anne's Health and Safety Policy Title of Policy: 4.01 St. Anne s Health and Safety Policy Issue date: July 2016 Version number: V5.0 Ratified by: H&S Committee 27 th July 2016 Expiry date: July
More informationDIRECTIVES. COUNCIL DIRECTIVE 2009/71/EURATOM of 25 June 2009 establishing a Community framework for the nuclear safety of nuclear installations
L 172/18 Official Journal of the European Union 2.7.2009 DIRECTIVES COUNCIL DIRECTIVE 2009/71/EURATOM of 25 June 2009 establishing a Community framework for the nuclear safety of nuclear installations
More informationProcedure for handling applications for authorisation and review reports under REACH
Procedure for handling applications for authorisation and review reports under REACH 1. Purpose This procedure describes how to handle applications for authorisation (AfA) as established by the REACH Regulation
More informationEUROPEAN PARLIAMENT Committee on the Environment, Public Health and Food Safety
EUROPEAN PARLIAMT 2009-2014 Committee on the Environment, Public Health and Food Safety 2012/0266(COD) 12.4.2013 ***I DRAFT REPORT on the proposal for a regulation of the European Parliament and of the
More informationRQIA Provider Guidance Independent Clinic Private Doctor Service
RQIA Provider Guidance 2017-2018 Independent Clinic Private Doctor Service www.r qia.org.uk A s s u r a n c e, C h a l l e n g e a n d I m p r o v e m e n t i n H e a l t h a n d S o c i a l C a r e What
More informationREPORTING OF REACH IMPLEMENTATION
National Supervisory Authority for Welfare and Health Finnish Environment Institute Ref. Ares(2011)183072-18/02/2011 REPORTING OF REACH IMPLEMENTATION 2007 2009 FINLAND 28 MAY2010 MS REACH Reporting Questionnaire
More informationDIRECTIVE 2009/148/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL
L 330/28 Official Journal of the European Union 16.12.2009 DIRECTIVE 2009/148/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 30 November 2009 on the protection of workers from the risks related to
More informationHealth and Safety Authority. Function and Scope of REACH and CLP Helpdesks
Rev 1. June 2009 Health and Safety Authority Function and Scope of REACH and CLP Helpdesks Introduction The EU Regulation for Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
More informationRQIA Provider Guidance Day Care Settings
RQIA Provider Guidance 2016-17 Day Care Settings www.r qia.org.uk A s s u r a n c e, C h a l l e n g e a n d I m p r o v e m e n t i n H e a l t h a n d S o c i a l C a r e What we do The Regulation and
More informationGuidance on the preparation of dossiers for harmonised classification and labelling (CLH) under Regulation (EC) No.
Guidance on the preparation of dossiers for harmonised classification and labelling (CLH) under Regulation (EC) No. 1272/2008 DRAFT LEGAL NOTICE This document contains guidance to the preparation of dossiers
More informationAUDIT REPORT. Audit of Official Controls carried out by the Health Service Executive (Regulation (EC) No 853/2004)
AUDIT REPORT Audit of Official Controls carried out by the Health Service Executive (Regulation (EC) No 853/2004) AUDIT REPORT Audit of Official Controls carried out by the Health Service Executive (Regulation
More informationRole Profile Medical Officer- Medical Devices
Role Profile Medical Officer- Medical Devices ROLE SUMMARY The Medical Officer role will be within the Medical Devices department. Reporting to the Deputy Director Medical Devices, the role of the Medical
More informationLEGISLATIVE ACTS AND OTHER INSTRUMENTS COUNCIL DIRECTIVE establishing a Community framework for the nuclear safety of nuclear installations
COUNCIL OF THE EUROPEAN UNION Brussels, 23 June 2009 (OR. en) 10667/09 Interinstitutional File: 2008/0231 (CNS) ATO 63 LEGISLATIVE ACTS AND OTHER INSTRUMTS Subject: COUNCIL DIRECTIVE establishing a Community
More informationGiuseppe Casale International Training Centre of the ILO Director of the Turin School of Development Secretary General ISLSSL
Giuseppe Casale International Training Centre of the ILO Director of the Turin School of Development Secretary General ISLSSL NATIONAL OSH POLICY National OSH Committee PUBLIC AUTHORITIES INSURANCE AND
More information1.1 About the Early Childhood Education and Care Directorate
Contents 1. Introduction... 2 1.1 About the Early Childhood Education and Care Directorate... 2 1.2 Purpose of the Compliance Policy... 3 1.3 Authorised officers... 3 2. The Directorate s approach to regulation...
More informationIntertek Health, Environmental & Regulatory Services
Intertek Health, Environmental & Regulatory Services Vai dove Ti porta la Chimica Go where the markets for Chemicals are! Workshop Centro REACH - 3 rd December 2014 Turkey - a country moving towards Europe
More informationSummers-Inman Group Health and Safety Policy SUMMERS-INMAN GROUP HEALTH AND SAFETY POLICY. Revision -
SUMMERS-INMAN GROUP HEALTH AND SAFETY POLICY 4 th November 2015 1 Table of Contents 1. Revision History... 5 2. Health and Safety Policy Statement... 7 3. Organisation... 9 Managing Director... 9 Group
More informationTERMS OF REFERENCE FOR IMPEL PROJECT
TERMS OF REFERENCE FOR IMPEL PROJECT * Please read the supporting notes before filling in each section of this form. 1. Project details Name of project IMPEL-TFS Prosecutor Project 2 2013/24 The ToR may
More informationRegulation on the implementation of the European Economic Area (EEA) Financial Mechanism
the European Economic Area (EEA) Financial Mechanism 2009-2014 adopted by the EEA Financial Mechanism Committee pursuant to Article 8.8 of Protocol 38b to the EEA Agreement on 13 January 2011 and confirmed
More informationRQIA Provider Guidance Independent Clinic Private Doctor Service
RQIA Provider Guidance 2016-17 Independent Clinic Private Doctor Service www.r qia.org.uk A s s u r a n c e, C h a l l e n g e a n d I m p r o v e m e n t i n H e a l t h a n d S o c i a l C a r e What
More information***I DRAFT REPORT. EN United in diversity EN. European Parliament 2018/0018(COD)
European Parliament 2014-2019 Committee on the Environment, Public Health and Food Safety 4.5.2018 2018/0018(COD) ***I DRAFT REPORT on the proposal for a regulation of the European Parliament and of the
More informationDRAFT OPINION. EN United in diversity EN. European Parliament 2018/0018(COD) of the Committee on Industry, Research and Energy
European Parliament 2014-2019 Committee on Industry, Research and Energy 2018/0018(COD) 13.4.2018 DRAFT OPINION of the Committee on Industry, Research and Energy for the Committee on the Environment, Public
More informationMEDICINES CONTROL COUNCIL
MEDICINES CONTROL COUNCIL GUIDELINES FOR RECALL/ WITHDRAWAL OF MEDICINES This document has been prepared to serve as a recommendation to applicants regarding the recalls of medicines, and the Medicines
More informationReservation of Powers to the Board & Delegation of Powers
Reservation of Powers to the Board & Delegation of Powers Status: Draft Next Review Date: March 2014 Page 1 of 102 Reservation of Powers to the Board & Delegation of Powers Issue Date: 5 April 2013 Document
More informationHR Services. Management of Health and Safety at Work Regulations (MHSW) 1999
HR Services Management of Health and Safety at Work Regulations (MHSW) 1999 This policy is a sub-policy of the main University Health and Safety Policy Statement The Management of Health and Safety at
More informationGENERAL STATEMENT OF SAFETY POLICY
THE SOUTHERN EDUCATION & LIBRARY BOARD GENERAL STATEMENT OF SAFETY POLICY POLICY OBJECTIVE: The objective of this Policy is to ensure, so far as is reasonably practicable, that no person is placed in a
More informationHealth and Safety Policy Part 1 Policy and organisation
Health and Safety Policy Part 1 Policy and organisation ICO H&S Policy Policy and organisation, June 2016 Page 1 of 5 1. Scope 1.1 The Health and Safety policy applies to all employees of the Information
More informationEUCERD RECOMMENDATIONS QUALITY CRITERIA FOR CENTRES OF EXPERTISE FOR RARE DISEASES IN MEMBER STATES
EUCERD RECOMMENDATIONS QUALITY CRITERIA FOR CENTRES OF EXPERTISE FOR RARE DISEASES IN MEMBER STATES 24 OCTOBER 2011 INTRODUCTION 1. THE EUROPEAN CONTEXT Centres of expertise (CE) and European Reference
More informationCOUNCIL OF THE EUROPEAN UNION. Brussels, 29 May /06 COSDP 376 PESC 460 CIVCOM 207 FIN 207 CSC 26 CAB 19 BUDGET 27
COUNCIL OF THE EUROPEAN UNION Brussels, 29 May 2006 9490/06 COSDP 376 PESC 460 CIVCOM 207 FIN 207 CSC 26 CAB 19 BUDGET 27 "I/A" ITEM NOTE From : PSC To : Coreper/Council Subject : Policy of the European
More informationLISAM SYSTEMS REACH Compliant SDSs: What s Changed and What s Coming
REACH Compliant SDSs: What s Changed and What s Coming Simon Bradshaw, June 2016 REACH Compliant SDSs: Structure, Content and Requirements Simon Bradshaw, June 2016 REACH... Regulation 1907/2006 Amendment
More informationFinal Draft Agenda Sixteenth meeting of the Forum for Exchange of Information on Enforcement (Forum-16) October 2013
18 October 2013 ECHA/Forum-16/2013/A/final Final Draft Agenda Sixteenth meeting of the Forum for Exchange of Information on Enforcement (Forum-16) 28-31 October 2013 European Chemicals Agency Helsinki,
More informationAcademy Health and Safety Policy 2017/2018
Academy Health and Safety Policy 2017/2018 Academy Name: Summerhill Academy Implementation Date: September 2017 Version: 1 History of Policy Changes Date Page Change Reason for Change September 2015 October
More informationJob Description. Ensure that patients are offered appropriate creative and diverse activities within a therapeutic environment.
Job Description POST: HOURS: ACCOUNTABLE TO: REPORTS TO: RESPONSIBLE FOR: Complementary Therapy Coordinator 30 37.5 hours Head of Nursing & Quality Day Therapy Clinical Lead Volunteer Complementary Therapists
More informationEUCERD RECOMMENDATIONS on RARE DISEASE EUROPEAN REFERENCE NETWORKS (RD ERNS)
EUCERD RECOMMENDATIONS on RARE DISEASE EUROPEAN REFERENCE NETWORKS (RD ERNS) 31 January 2013 1 EUCERD RECOMMENDATIONS ON RARE DISEASE EUROPEAN REFERENCE NETWORKS (RD ERNS) INTRODUCTION 1. BACKGROUND TO
More informationHealth & Safety Policy
Health & Safety Policy DATE ISSUED: 1 April 2014 DATE TO BE REVIEWED: 1 April 2014 Health & Safety Policy Page 1 of 11 CONTENTS POLICY OVERVIEW 1 Introduction 2 Purpose 3 Who This Policy Applies To 4 Key
More informationPrivacy Code for Consumer, Customer, Supplier and Business Partner Data
Privacy Code for Consumer, Customer, Supplier and Business Partner Data Introduction JACOBS DOUWE EGBERTS is committed to the protection of personal data of its Consumer, Customers, Suppliers and Business
More informationI. Preamble: II. Parties:
I. Preamble: MEMORANDUM OF UNDERSTANDING BETWEEN THE FEDERAL COMMUNICATIONS COMMISSION AND THE FOOD AND DRUG ADMINISTRATION CENTER FOR DEVICES AND RADIOLOGICAL HEALTH The Food and Drug Administration (FDA)
More informationApplication for Recognition or Expansion of Recognition
Application for Recognition or Expansion of Recognition Notes for applicants All Applicants Should Read This Section This form is for applicants who are: o applying to become a recognised awarding organisation
More informationHEALTH AND SAFETY MANAGEMENT AT UWE
HEALTH AND SAFETY MANAGEMENT AT UWE Introduction This document sets out the University s strategic approach to health and safety management. It contains the Statement of Intent that outlines the University
More informationHEALTH AND SAFETY POLICY
HEALTH AND SAFETY POLICY Policy Statement, Specific Health and Safety Policies/ Safe Working Procedures Version 2 Page 1 of 11 General Health and Safety Policy Statement 1. Objectives 2. Responsibilities
More informationChanges to Chemical Labels and SDS - Speaker s notes
Slide 1 Changes to Chemical Labels and SDS Title slide. Slide 2 Changes to labels and SDS This presentation is intended to help those who need to give information about changes to the way that chemical
More informationGuidance on Scientific Research and Development (SR&D) and Product and Process Orientated Research and Development (PPORD)
G U I D A N C E Guidance on Scientific Research and Development (SR&D) and Product and Process Orientated Research and Development (PPORD) Version 2.1 October 2017 2 Guidance on Scientific Research and
More informationHealth Safety BARNSLEY AN EMPLOYEE S GUIDE TO THE BARNSLEY MBC HEALTH & SAFETY POLICY. Metropolitan Borough Council
Health & Safety P O L I C Y AN EMPLOYEE S GUIDE TO THE BARNSLEY MBC HEALTH & SAFETY POLICY BARNSLEY Metropolitan Borough Council DUTIES AND RESPONSIBILITIES 1 ELECTED MEMBERS Elected Members have a responsibility
More informationHigh Level Pharmaceutical Forum
High Level Pharmaceutical Forum 2005-2008 Final Conclusions and Recommendations of the High Level Pharmaceutical Forum On 2 nd October 2008, the High Level Pharmaceutical Forum agreed on the following
More informationREACH Pre-registration Questions and Answers
REACH Pre-registration Questions and Answers (RELEASE 5) You may continue to manufacture, import or use a chemical only if it is pre-registered and registered in time! Reference: ECHA-08-QA-01.5-EN Date:
More informationOfficial Journal of the European Union. (Non-legislative acts) REGULATIONS
4.1.2017 L 1/1 II (Non-legislative acts) REGULATIONS COMMISSION IMPLEMTING REGULATION (EU) 2017/1 of 3 January 2017 on procedures for watercraft identification under Directive 2013/53/EU of the European
More informationNotice of Proposed Amendment Requirements for apron management services at aerodromes
European Aviation Safety Agency Rulemaking Directorate Notice of Proposed Amendment 2013-24 Requirements for apron management services at aerodromes RMT.0485 AND RMT.0465 18.12.2013 EXECUTIVE SUMMARY This
More informationHEALTH & SAFETY POLICY CONTENTS
Health & Safety Policy Statement of Intent Health and Safety responsibilities Health and Safety rules Warning signs Working conditions Fire precautions Accidents and Incidents Health Hygiene Protective
More informationCREATIVE EUROPE ( ) Culture Sub-programme. Call for proposals : EACEA 32/2014 : European cooperation projects
CREATIVE EUROPE (2014-2020) Culture Sub-programme Call for proposals : EACEA 32/2014 : European cooperation projects Implementation of the Culture Sub-programme schemes: European cooperation projects.
More informationJob Description & Person Specification Job Title:
Job Description & Person Specification Job Title: Senior Care Worker Company: Agincare UK Ltd Reporting to: Field Care Supervisor or Registered Manager PURPOSE To support the Field Care Supervisor to lead,
More informationResearch Governance Framework 2 nd Edition, Medicine for Human Use (Clinical Trial) Regulations 2004
Title: Outcome Statement: Research Auditing and Monitoring Procedures Researchers in the Trust and research partners will be informed about the requirements and procedures involved in research audit and
More informationPART A. In order to achieve its objectives, this Code embodies a number of functional requirements. These include, but are not limited to:
PART A MANDATORY REQUIREMENTS REGARDING THE PROVISIONS OF CHAPTER XI-2 OF THE INTERNATIONAL CONVENTION FOR THE SAFETY OF LIFE AT SEA, 1974, AS AMENDED 1 GENERAL 1.1 Introduction This part of the International
More informationHEALTH AND SAFETY POLICY
NHS GREATER GLASGOW AND CLYDE HEALTH AND SAFETY POLICY November 2015 Lead Manager: K. Fleming Head of Health and Safety Responsible Director A. MacPherson Director of Human Resources and Organisational
More informationRestoration to the register: Guidance for applicants and committees
Restoration to the register: Guidance for applicants and committees August 2017 The text of this document (but not the logo and branding) may be reproduced free of charge in any format or medium, as long
More informationInspection of residential family centres
Inspection of residential family centres Framework for inspection from April 2013 This document sets out the framework and guidance for the inspection of residential family centres from April 2013. It
More informationA BRIEF EXPLANATION OF THE LEGAL OBLIGATIONS UNDER LEGIONELLOSIS LEGISLATION
A BRIEF EXPLANATION OF THE LEGAL OBLIGATIONS UNDER LEGIONELLOSIS LEGISLATION Prepared by Aqua Legion UK Ltd Suite 335 Kemp House 152-160 City Road London EC1V 2NX Tel: +44 (0) 20 8555 3797 Fax: +44 (0)
More informationSDS and what is new under REACH and EU GHS? PRISM2 Workshop Promoting Resposibility in SME s 08 April Slovakia. L. Heezen
SDS and what is new under REACH and EU GHS? PRISM2 Workshop Promoting Resposibility in SME s 08 April Slovakia L. Heezen Why do we need GHS? Substance - oral toxicity LD 50 = 257 mg/kg GHS Transport EU
More information25/02/18 THE SOCIAL CARE WALES (REGISTRATION) RULES 2018
25/02/18 THE SOCIAL CARE WALES (REGISTRATION) RULES 2018 April 2018 The regulation of the registration and fitness to practise of the social care workforce by Social Care Wales is governed by three types
More informationZAMBIA MEDICINES REGULATORY AUTHORITY EMPLOYMENT OPPORTUNITY
ZAMBIA MEDICINES REGULATORY AUTHORITY EMPLOYMENT OPPORTUNITY The Zambia Medicines Regulatory Authority (ZAMRA) was set up by the Medicines and Allied Substances Act (No. 3) of 2013 as a statutory body
More informationHealth and Safety Strategy
NHS Newcastle Gateshead Clinical Commissioning Group Health and Safety Strategy Document Status Equality Impact Assessment Document Ratified/Approved By Final No impact Quality, Safety and Risk Committee
More informationSTRATHEARN SCHOOL. Draft HEALTH & SAFETY POLICY
STRATHEARN SCHOOL Draft HEALTH & SAFETY POLICY January 2016 CONTENTS Page Management Chain 3 Statement of General Policy 4-5 Organisation Responsibilities: 6 All Staff 6 Safety Representative 6-7 Heads
More informationThis document is meant purely as a documentation tool and the institutions do not assume any liability for its contents
2012R0036 EN 24.07.2013 012.001 1 This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents B COUNCIL REGULATION (EU) No 36/2012 of 18 January
More informationForeword... 1 Introduction... 2 Context... 2 Key Messages from the Review... 5 Aim and Objectives of the HSA Plan for the Healthcare Sector...
Health and Safety Authority Five Year Plan for the Healthcare Sector 2010 2014 Working to create a National Culture of Excellence in Workplace Safety, Health and Welfare for Ireland Contents Foreword......................................
More informationCouncil, 25 September 2014
Council, 25 September 2014 Directive 2013/55/EU the revised Recognition of Professional Qualifications (RPQ) Directive challenges and opportunities for the Health and Care Professions Council (HCPC) Executive
More informationHealth and Safety Policy and Managerial Responsibilities
Health and Safety Policy and Managerial Responsibilities 1.0 Purpose This document outlines the policies, procedures and practices governing the manner in which the Royal Conservatoire of Scotland manages
More informationPHYSIOTHERAPY ACT STANDARDS AND DISCIPLINE REGULATIONS
c t PHYSIOTHERAPY ACT STANDARDS AND DISCIPLINE REGULATIONS PLEASE NOTE This document, prepared by the Legislative Counsel Office, is an office consolidation of this regulation, current to July 11, 2009.
More information25/02/18 THE SOCIAL CARE WALES (REGISTRATION) RULES 2018
25/02/18 THE SOCIAL CARE WALES (REGISTRATION) RULES 2018 April 2018 0 The regulation of the registration and fitness to practise of the social care workforce by Social Care Wales is governed by three types
More informationPractice Guidance: Large Scale Investigations
Practice Guidance: Large Scale Investigations Version: Version 1: April 2014 Ratified by: Leeds Safeguarding Adults Board Date ratified: April 2014 Author/Originator of title Safeguarding Policy, Protocols
More informationPractising as a midwife in the UK
Practising as a midwife in the UK An overview of midwifery regulation CONTENTS Introduction 3 Section 1: Education 4 Section 2: Joining the register and maintaining registration 6 Section 3: Standards
More informationRQIA Provider Guidance Nursing Homes
RQIA Provider Guidance 2016-17 Nursing Homes www.r qia.org.uk A s s u r a n c e, C h a l l e n g e a n d I m p r o v e m e n t i n H e a l t h a n d S o c i a l C a r e What we do The Regulation and Quality
More informationHealth and Safety Roles, Responsibilities and Organisation
Health and Safety Roles, Responsibilities and Organisation Document Control Information Published Document Name: safety-organisation-gn.pdf Date issued: November 2015 Version: 3.0 Previous Review Dates:
More informationEducation and Training Committee, 5 June 2014
Education and Training Committee, 5 June 2014 Directive 2013/55/EU the revised Recognition of Professional Qualifications (RPQ) Directive challenges and opportunities for the Health and Care Professions
More informationOrdinance on Good Laboratory Practice (OGLP)
English is not an official language of the Swiss Confederation. This translation is provided for information purposes only and has no legal force. Ordinance on Good Laboratory Practice (OGLP) 813.112.1
More informationREACH Forum, Compliance Control of REACH and CLP Regulations
REACH Forum, Compliance Control of REACH and CLP Regulations Szilvia Deim Vice-Chair of the Forum Forum for Exchange of Information on Enforcement 4 September 2018, Bratislava 1 Forum as a unique body
More informationHealth & Safety Policy
Health & Safety Policy Title Health & Safety Policy Author Head of Health & Safety Approved by Management Board Issue date 1 st May 2015 Review date March 2018 (or sooner if necessary) Links to other procedures
More informationJob Description. CNS Clinical Lead
Job Description CNS Clinical Lead POST: BASE: ACCOUNTABLE TO: REPORTS TO: RESPONSIBLE FOR: CNS Clinical Lead St John s Hospice Head of Nursing and Quality Head of Nursing and Quality Community Clinical
More informationREPUBLIC OF LITHUANIA LAW ON SAFETY AND HEALTH AT WORK. 1 July 2003 No IX-1672 Vilnius (As last amended on 2 December 2010 No.
REPUBLIC OF LITHUANIA LAW ON SAFETY AND HEALTH AT WORK 1 July 2003 No IX-1672 Vilnius (As last amended on 2 December 2010 No. XI-1202) PART I GENERAL PROVISIONS CHAPTER I SCOPE, BASIC CONCEPTS AND APPLICATION
More informationFinal Report. Recommendations on outsourcing to cloud service providers EBA/REC/2017/ December 2017
EBA/REC/2017/03 20 December 2017 Final Report Recommendations on outsourcing to cloud service providers Contents 1. Executive summary 3 2. Background and rationale 5 3. Recommendations 8 5. Accompanying
More informationGDPR DATA PROCESSING ADDENDUM. (Revision March 2018)
GDPR DATA PROCESSING ADDENDUM (Revision March 2018) From 25 May 2018 the GDPR obliges a Controller to have a written agreement containing prescribed provisions with any Processor that it uses. This General
More informationCLP the implementation of GHS in the EU Facts and practical advice
CLP the implementation of GHS in the EU Facts and practical advice Seminar on the latest trend regarding revised CSCL, REACH and CLP 30 March 2010, Tokyo Gabriele Schöning ECHA Classification Unit Content
More informationQUALITY COMMITTEE. Terms of Reference
QUALITY COMMITTEE Terms of Reference This Committee will report to NHS Halton CCG Governing Body on the development, improvement and monitoring of all areas of quality. This will include clinical effectiveness,
More informationAnnual review of performance 2016/17. General Osteopathic Council
Annual review of performance 216/17 General Osteopathic Council About the Professional Standards Authority The Professional Standards Authority for Health and Social Care 1 promotes the health, safety
More information