Interpretation and Implications of the European Commission Recommendation on the Definition of Nanomaterial
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Reports of Cases
Report s of C ases OPINION OF ADVOCATE GENERAL BOBEK delivered on 17 March 2016 1 Case C-592/14 European Federation for Cosmetic Ingredients v Secretary of State for Business, Innovation and Skills (Request for a preliminary ruling from the High Court of Justice of England & Wales, Queen’s Bench Division (Administrative Court)(United Kingdom)) (Request for a preliminary ruling — Internal market — Regulation No 1223/2009 — Article 18(1)(b) — Cosmetic products — Cosmetic ingredients — Ban on the marketing of cosmetic ingredients having been tested on animals)) Table of contents I – Introduction ................................................................................... 2 II – Legal framework ............................................................................... 3 A – EU law .................................................................................. 3 B – National law ............................................................................. 4 C – WTO law ............................................................................... 4 III – Facts, procedure and questions referred ......................................................... 5 IV – Assessment .................................................................................... 6 A – Preliminary considerations ................................................................ 6 B – Analysis of Article 18(1)(b) ............................................................... 7 1. Introduction ........................................................................ -
INCEPTION IMPACT ASSESSMENT Revision of EU Legislation On
Ref. Ares(2021)2969734 - 04/05/2021 INCEPTION IMPACT ASSESSMENT Inception Impact Assessments aim to inform citizens and stakeholders about the Commission's plans in order to allow them to provide feedback on the intended initiative and to participate effectively in future consultation activities. Citizens and stakeholders are in particular invited to provide views on the Commission's understanding of the problem and possible solutions and to make available any relevant information that they may have, including on possible impacts of the different options. TITLE OF THE INITIATIVE Revision of EU legislation on hazard classification, labelling and packaging of chemicals LEAD DG (RESPONSIBLE UNIT) ENV.B2, GROW.F2 LIKELY TYPE OF INITIATIVE Legislative initiative INDICATIVE PLANNING Q2 2022 ADDITIONAL INFORMATION https://ec.europa.eu/environment/strategy/chemicals-strategy_en The Inception Impact Assessment is provided for information purposes only. It does not prejudge the final decision of the Commission on whether this initiative will be pursued or on its final content. All elements of the initiative described by the Inception impact assessment, including its timing, are subject to change. A. Context, Problem definition and Subsidiarity Check Context The Commission’s European Green Deal1 sets a high ambition for zero pollution leading to a toxic-free environment. One of the first deliverables is the Chemicals Strategy for Sustainability: Towards a Toxic-free Environment2 adopted on 14 October 2020. The objectives of the strategy are to achieve a legitimate higher level of protection of citizens and of the environment against hazardous chemicals. It is also an opportunity to encourage innovation for the development of safe and sustainable alternatives and to promote the EU industry as a global frontrunner in the chemicals production and use. -
Information Gathering for CLP Classification
132 ANN IST SUPER SANITÀ 2011 | VOL. 47, NO. 2: 132-139 DOI: 10.4415/ANN_11_02_03 Information gathering for CLP classification Ida Marcello(a), Felice Giordano(b) and Francesca Marina Costamagna(a) 1272/2008 (a)Centro Nazionale Sostanze Chimiche, Istituto Superiore di Sanità, Rome, Italy ON (b) I Dipartimento di Sanità Pubblica e Malattie Infettive, Sapienza Università di Roma, Rome, Italy T A EGUL Summary. Regulation 1272/2008 includes provisions for two types of classification: harmonised classi- R fication and self-classification. The harmonised classification of substances is decided at Community level and a list of harmonised classifications is included in the Annex VI of the classification, labelling CLP and packaging Regulation (CLP). If a chemical substance is not included in the harmonised classifi- HE cation list it must be self-classified, based on available information, according to the requirements of T Annex I of the CLP Regulation. CLP appoints that the harmonised classification will be performed for carcinogenic, mutagenic or toxic to reproduction substances (CMR substances) and for respira- tory sensitisers category 1 and for other hazard classes on a case-by-case basis. The first step of clas- sification is the gathering of available and relevant information. This paper presents the procedure for gathering information and to obtain data. The data quality is also discussed. Key words: hazardous substances, European Union, information systems, classification, globally harmonized system. Riassunto (Raccolta di informazioni per la classificazione in accordo con il Regolamento CLP). Il Regolamento sulla classificazione, etichettatura e imballaggio di sostanze e miscele (CLP) considera due tipi di classifi- cazione: la classificazione armonizzata e l’autoclassificazione. -
REACH Annex II SDS Changes Christine Lepisto SCHC Fall Meeting, 2020
REACH Annex II SDS Changes Christine Lepisto SCHC Fall Meeting, 2020 AGENDA REACH Annex II SDS Changes The Basics: What, Why, When? Change drivers: UN GHS Revisions 6 and 7 CLP Regulation: Adaptations to Technical Progress CLP Regulation: NEW Annex VIII on Poison Centre Notification REACH Amendments: Registration of Nanoforms REACH and the European Union framework on endocrine disruptors REACH: Evolving trends in Substances of Very High Concern Accumulated effects on Section 3 of the SDS 1-Nov-20 © C. Lepisto, Chemical Safety Consulting, 2020 3 REACH Annex II SDS Changes WHAT, WHY, WHEN? 1-Nov-20 © C. Lepisto, Chemical Safety Consulting, 2020 4 THE BASICS What – Amendment to REACH • COMMISSION REGULATION (EU) 2020/878 of 18 June 2020 amending Annex II to Regulation (EC) No 1907/2006 of the European Parliament and of the Council concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) 1-Nov-20 © C. Lepisto, Chemical Safety Consulting, 2020 5 THE BASICS Why – the Drivers • Revision of GHS: 12th ATP of CLP • The 12th ATP of CLP sets GHS 6th and 7th Revised edition requirements in effect by 17 October 2020. • Other changes related to CLP • Specific concentration limits, multiplying factors, acute toxicity estimates • Annex VIII Poison Centre Notification Unique Formula Identifier (UFI) • Related to REACH Annexes I, III and VI to XII • Nanoforms • European Union framework on endocrine disruptors • Emerging substances of very high concern (SVHCs) 1-Nov-20 © C. Lepisto, Chemical Safety Consulting, 2020 6 THE BASICS When – and “Really, when?” • SHALL APPLY FROM • DEROGATION: Safety data sheets not complying with the Annex to this Regulation may continue to be provided until… CEFIC:ECHA: 31 Dec Still 2022 NEWdiscussing,forReally, new and or IMPROVED! when? existing answer in SDSSDS guidance 1-Nov-20 © C. -
Etibor-68 Safety Data Sheet
ETİBOR-68 SAFETY DATA SHEET Date of initial Issue : March 2007 Revision No : 08.2 Date of Revision : February 2019 ETİ MADEN İŞLETMELERİ GENEL MÜDÜRLÜĞÜ Ayvalı Mah. Halil Sezai Erkut Cad. Afra Sok. No: 1/A 06010 Keçiören/Ankara TÜRKİYE SECTION 1. Identification of the Substance and the Company 1.1. Product identifier Substance name : Disodium tetraborate, anhydrous Trade name : ETİBOR-68 (Anhydrous borax) Chemical name/synonyms: Anhydrous borax, dehydrated borax, disodium tetraborate anhydrous Index N° : 005-011-00-4 CAS N° : 1330-43-4 EC N° : 215-540-4 REACH Registration number: 01-2119490790-32-0002 1.2. Relevant identified uses of the substance and uses advised against Relevant identified uses The product is used in industrial manufacturing and formulation, among others in: - Metallurgical Fluxes - Glass - Fiberglass - Ceramics - Fertilizers - Flame retardants For area-specific use, see the exposure scenarios in the annex of this extended Safety Data Sheet (eSDS). Uses advised against Not applicable, there are no uses of Etibor-68 (Anhydrous borax) advised against. 1.3. Details of the supplier of the safety data sheet Importer Name : AB ETIPRODUCTS OY Address : Piispanportti 5, 02240 Espoo/FINLAND Phone No : + 358 9 819 444 40 Fax No : + 358 9 819 444 44 e-mail : [email protected] Manufacturer Name : ETİ MADEN İŞLETMELERİ GENEL MÜDÜRLÜĞÜ Address : Ayvalı Mah. Halil Sezai Erkut Cad. Afra Sok. No: 1/A 06010 Keçiören/Ankara TÜRKİYE Phone No : +90 312 294 20 00 Fax No : +90 312 232 71 84 1.4. Emergency phone number : +49 (0)6132-84463 (24-Hour-Number) GBK GmbH Page 2 of 14 SECTION 2. -
The CLP Regulation: Origin, Scope and Evolution
126 ANN IST SUPER SANITÀ 2011 | VOL. 47, NO. 2: 126-131 DOI: 10.4415/ANN_11_02_02 The CLP Regulation: origin, scope and evolution 1272/2008 ON I Paola Di Prospero Fanghella and Tiziana Catone T A Centro Nazionale Sostanze Chimiche, Istituto Superiore di Sanità, Rome, Italy EGUL R Summary. The CLP Regulation implements in the EU the UN Globally Harmonised System of Classification and Labelling applying the “building block approach”, that is taking on board the CLP hazard classes and categories which are close to the existing EU system in order to maintain the HE level of protection of human health and environment. This Regulation applies to all substances and T mixtures placed on the market and besides to classification, packaging and labelling it provides for the notification of the classification and labelling of substances to the Classification & Labelling Inventory established by ECHA. It came into force on 20 January 2009 but a transitional period is foreseen until 1 June 2015 for the full application. At the end of this period the “substance” and “preparation” Directives (respectively 67/548/EEC and 99/45/EC) will be repealed. Key words: GHS, CLP, classification and labelling, C&L Inventory, CLP helpdesk, CLP notification. Riassunto (Il Regolamento CLP: origine, scopo ed evoluzione). Il Regolamento CLP traspone nel- l’Unione Europea il sistema armonizzato globale delle Nazioni Unite applicando il criterio del building block approach che consente di adottare alcune classi e categorie di pericolo simili a quelle preesistenti nell’attuale sistema UE per mantenere il livello attuale di protezione della salute umana e dell’ambiente. -
Situation in the Different Sectors
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Archive of European Integration COMMISSION OF THE EUROPEAN COMMUNITIES Brussels, 18.11.2008 SEC(2008) 2854 COMMISSION STAFF WORKING DOCUMENT accompanying the 25th ANNUAL REPORT ON MONITORING THE APPLICATION OF COMMUNITY LAW (2007) SITUATION IN THE DIFFERENT SECTORS {COM(2008) 777 final} {SEC(2008) 2855} EN EN TABLE OF CONTENTS 1 ENTERPRISE AND INDUSTRY ............................................................................. 16 1.1 General introduction...................................................................................................16 1.2 Automotive Industry.................................................................................................. 17 1.2.1 Current position.......................................................................................................... 17 1.2.2 Changes underway..................................................................................................... 18 1.2.3 Evaluation .................................................................................................................. 18 1.3 Chemicals................................................................................................................... 19 1.3.1 Dangerous substances and preparations..................................................................... 19 1.3.2 Fertilizers and detergents ........................................................................................... 20 1.3.3 Drug precursors......................................................................................................... -
2019) XXX Draft COMMISSION DELEGATED REGULATION (EU
Ref. Ares(2019)4744568 - 22/07/2019 EUROPEAN COMMISSION Brussels, XXX […](2019) XXX draft COMMISSION DELEGATED REGULATION (EU) …/... of XXX amending Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures as regards information relating to emergency health response (Text with EEA relevance) This draft has not been adopted or endorsed by the European Commission. Any views expressed are the preliminary views of the Commission services and may not in any circumstances be regarded as stating an official position of the Commission. EN EN EXPLANATORY MEMORANDUM 1. CONTEXT OF THE DELEGATED ACT According to Article 45(1) of the CLP Regulation, Member States' appointed bodies shall receive information from importers and downstream users on the hazardous chemical mixtures they place on the market. Commission Regulation (EU) No 2017/542 amended the CLP Regulation (EC) No 1272/2008 by adding an Annex harmonising the information to be provided relating to emergency health response (“Annex VIII”). Annex VIII was adopted in March 2017 and was intended to become applicable on 1 January 2020. The Commission is proposing an amendment to Annex VIII before its applicability date that would contain uncontentious clarifications of the text, so as to allow a more streamline interpretation of the text, improve internal coherence and mitigate some unintended consequences made apparent only after the adoption of the Annex. The Commission is also proposing an amendment of the first compliance deadline (identical with the applicability date of Annex VIII) from 1 January 2020 to 1 January 2021 given that there have been calls for more extensive amendments to Annex VIII before its applicability date, for reasons of workability concerns. -
A Guide to What Is a Medicinal Product
A guide to what is a medicinal product MHRA Guidance Note 8 March 2020 1 A guide to what is a medicinal product © Crown Copyright 2020 MHRA 10 South Colonnade Canary Wharf, London E14 4PU Published by MHRA 2020 (Certain Appendices may have been updated at different times) Applications for reproduction should be made in writing to: The Copyright Unit Her Majesty’s Stationery Office St Clements House 2-16 Colegate Norwich NR3 1BQ This MHRA Guidance Note should not be taken as a complete or definitive statement of the law. It is not intended as a substitute for legal or other professional advice. The MHRA accepts no liability for any loss or damage caused, arising directly, or indirectly, in connection with reliance on the contents of this Guidance Note. 2 Contents Page Introduction 5 1. What are Borderline Products? 5 2. MHRA policy and practice 5 3. How does the MHRA determine as to whether the product is a 6 medicinal product 4. What is a medicinal product? 6 • Definition • Meaning of Disease 5. Advertising 7 • Regulations • Internet advertising 6. Deciding factors when determining the regulatory status of a product 8 7. Products that are not classified as medicines under the “functional” 10 limb of the definition of a medicinal product 8. Is my product a herbal medicinal product? 11 9. Is my product a homeopathic medicinal product? 11 10. What claims can I make for my product? 12 • Claims to treat or prevent disease • Claims to “maintain” health • Cosmetic claims • Food claims 11. Products judged to be non-medicinal 14 12. -
IC L International Chemical Regulatory and Law Review
Volume 4 | Number 1 ICRL 1 2021 International Chemical Regulatory IC L and Law Review Articles The European Commission's Chemicals Strategy for Sustainability: The Challenge of Matching Political Aspirations with Workable Regulatory Outcomes Lawrie McLaren, Roland Moore and Alexander Majer The Concept of Essential Use to Regulate Chemicals: Legal Considerations Jean-Philippe Montfort Reports Chemical Legislation in Serbia: An Overview Alja Livio Torkhani REACH Restriction and Authorisation are Driving Replacement of Harmful Chemicals: Know Your Substances Before It Is Too Late Jaime Sales and Dieter Drohmann REACH Registration of Polymers: Identifying Polymers of Low Concern Jeffrey Hafer Case Notes The End of the “SONC” Saga: Judgment of the Court of Justice of 21 January 2021 in Case C-471/18 P, Federal Republic of Germany v ECHA Eléonore Mullier and Andrea Bonavita GET EXPERTS ON YOUR SIDE You can focus on running your business – we help you overcome the regulatory barriers. Powered by TCPDF (www.tcpdf.org) • For more than 14 years your strategic partner to comply with O R - Tru s tee international and national chemical REACH CLP control legislation. Regulatory Data Sheets Only Representative Regulatory Training • Comprehensive expertise in global regulatory affairs, toxicology, LoA Management GLP & GMP Consulting risk assessment, environmental EH&S International Chemical Control Legislation sciences and data sharing. Permission granted to user: [email protected] Advocacy & Authorisation Supply Chain Compliance • Ensuring your compliance in the Biocides Global Chemical Inventory Notifications supply chain with our unique Labels OR-Trustee system – available for GHS Exposure Scenarios Consortia Management REACH, UK REACH and KKDIK. K-REACH Chemical Safety Assessment • One of the leading independent Food Contact regulatory affairs service providers Safety Data Sheets globally, with offices in Germany, Cosmetics Luxembourg, Korea, Switzerland, Spain, UK, USA and Turkey. -
Governance by Committee: the Role of Committees in European Policy Making and Policy
Governance by Committee: The Role of Committees in European Policy Making and Policy Research Paper 00/GHA Return to Introduction STATE OF THE ART REPORT CONTRACT NUMBER: HPSE-CT-1999-00019 PROJECT NUMBER: SERD-1999-00128 TITLE: GOVERNANCE BY COMMITTEE, THE ROLE OF COMMITTEES IN EUROPEAN POLICY-MAKING AND POLICY IMPLEMENTATION MAASTRICHT, MAY 2000 Table of Contents 1. General Introduction ................................................................................................................ 4 Subproject 1: The Standing Committees in the European Parliament 2.1..................Introduction ............................................................................................................... 6 2.2..................The Evolution of the European Parliament: From Consultative ............................... 6 Assembly to Co-legislator 2.2.1...............The EP as a Legislative Actor after Maastricht......................................................... 7 2.2.2...............EP and Council on an Even Footing after Amsterdam.............................................. 8 2.2.2.1. ..........The Streamlining of the Co-decision Procedure........................................................ 9 2.3..................The Role of EP Committees in the Legislative Process ............................................ 10 2.3.1...............Membership in EP Committees.................................................................................12 2.3.2...............Powers and Competences of EP Committees........................................................... -
2) Plans for Harmonisation with the Acquis Communautaire
2) Plans for harmonisation with the acquis communautaire a) Plans with regard to the remaining necessary harmonisation of the national legislative framework with the acquis communautaire / b) An overview of the measures and activities to be undertaken in order to establish or strengthen institutional structures and administrative capacities / c) Planned measures to achieve full compliance with the EU acquis Serbia will continue to actively promote opportunities for the cultural and creative sec- tor within the EU programmes. Serbia's participation in the Creative Europe Programme is strategic objective and Serbia is dedicated to this task. When Serbia becomes a member of the EU, it will be dedicated to participating in the European Heritage Label Programme, which promotes cultural monuments and localities that symbolize European values and ideals and common history, thus contribute to the strengthen- ing of intercultural dialogue and better understanding among young people. 3.27. ENVIRONMENT 3.27.1. State-of-play In December 2016, the negotiating group 27 received the Screening Report for Chapter 27 and was asked to submit a negotiating position for this chapter without initial criteria. In July 2017, on the basis of the Law on Ministries ("Official Gazette of the Republic of Ser- bia", No. 44/14, 14/15, 54/15 and 96/15 - other law), an independent Ministry of Environmental Protection was formed. The Ministry of Environmental Protection is the leading institution for Chapter 27, while responsibilities for certain regulations have been assigned to the Ministry of Agriculture, Forestry and Water Management, while some regulations have remained within the competence of ministries in which they were previously (Ministry of Construction, Transport and Infrastructure, Ministry of Interior, Ministry of Mining and Energy, Ministry of Health, Ministry of Justice).