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Regulation eu 2021 2470

Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (Text with EEA relevance. ) Durchführungsverordnung (EU) 2017/2470 der Kommission vom 20. Dezember 2017 zur Erstellung der Unionsliste der neuartigen Lebensmittel gemäß der. Commission Implementing Regulation (EU) 2017/2470 is up to date with all changes known to be in force on or before 20 November 2020. There are changes that may be brought into force at a future date. Changes to Legislation. Revised legislation carried on this site may not be fully up to date. Changes and effects are recorded by our editorial team in lists which can be found in the 'Changes.

Commission Implementing Regulation (EU) 2017/2470 of 20

COMMISSION IMPLEMENTING REGUL ATION (EU) 2017/2470 of 20 December 2017 est ablishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (Text with EEA relevance) THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation (EU) 2015/2283 of the. Commission Implementing Regulation (EU) 2017/2470, Introductory Text is up to date with all changes known to be in force on or before 20 November 2020. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations. Changes to Legislation . Revised legislation carried on this site may not be fully up to.

L 351/72 EN Official Journal of the European Unio

  1. B COMMISSION IMPLEMENTING REGULATION (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (Text with EEA relevance) (OJ L 351, 30.12.2017, p. 72) Amended by: Official Journal No page date M1 Commission Implementing Regulation (EU) 2018/460 of 20 March 2018 L 78 2.
  2. Commission Implementing Regulation (EU) 2017/2470, Division 1. is up to date with all changes known to be in force on or before 16 November 2020. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations. Changes to Legislation. Changes and effects yet to be applied by the editorial team are only.
  3. Commission Implementing Regulation (EU) 2017/2470, Article 2 is up to date with all changes known to be in force on or before 31 October 2020. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations. Changes to Legislation . Revised legislation carried on this site may not be fully up to date.

Union list of novel foods Food Safety - ec

  1. Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (Text with EEA relevance. ) Règlement d'exécution (UE) 2017/2470 de la Commission du 20 décembre 2017 établissant la liste de l'Union des nouveaux aliments conformément au.
  2. Commission Implementing Regulation (EU) 2019/1272 of 29 July 2019 correcting Implementing Regulation (EU) 2017/2470 establishing the Union list of novel foods and Implementing Decision (EU) 2017/2078 authorising an extension of use of yeast beta-glucans as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council. Commission Implementing Regulation.
  3. Commission Implementing Regulation (EU) 2019/1686 of 8 October 2019 authorising the extension of use of bovine milk basic whey protein isolate as a novel food under Regulation (EU) 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) 2017/2470 (Text with EEA relevance
  4. Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 Establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel food
  5. ation of novel food status in accordance with.
  6. Durchführungs­verordnung (EU) 2017/2470 der Kommission zur Erstellung der Unionsliste der neuartigen Lebensmittel gemäß der Verordnung (EU) 2015/2283 des Europäischen Parlaments und des Rates über neuartige Lebensmittel. Vom 20. Dezember 2017 (ABl. 2017 Nr. L 351/72), zul. geänd. durch Art. 1 der DVO (EU) 2020/1559 vom 26.10.2020 (ABl. 2020 Nr. L 357/7) Änderungshistorie. nicht.

EUR-Lex - 32019R1686 - EN - EUR-Le

On October 27, the European Commission revised the (EU) 2017/2470 new resource food list. The regulation authorized the new resource food Ecklonia cava phlorotannins, and revised the limit of Taxifolin-rich extract, three herbal root extracts (Cynanchum wilfordii Hemsley, Phlomis umbrosa Turcz and Angelica gigas Nakai), UV-treated mushrooms (Agaricus bisporus), UV-treated baker's yeast. Novel Food is defined as food that had not been consumed to a significant degree by humans in the EU before 15 May 1997, when the first Regulation on novel food came into force. 'Novel Food' can be newly developed, innovative food, food produced using new technologies and production processes, as well as food which is or has been traditionally eaten outside of the EU. Skip to main content. 2 Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (OJ 351, 30.12.2017, p. 72). 3 Regulation (EC) No 258/97 of the European Parliament and of the Council concerning novel foods and novel foods ingredients (OJ L 43, 14.2.1997.

Commission Implementing Regulation (EU) 973/2020 – FOOD in

Regulation (EU) 2017/2470 - lexparency

Commission Implementing Regulation (EU) 2018/2017 of 18 December 2018 authorising the placing on the market of syrup from Sorghum bicolor (L.) Moench as a traditional food from a third country under Regulation (EU) 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) 2017/2470 (OJ L323, 19.122018, page 4 Regulation (EU) 2017/2470 establishing the Union list of novel foods (OJ L 187, 24.7.2018, p. 1). EN 2 EN Article 5 of Regulation (EC) No 258/97 of the 5European Parliament and of the Council indicating a wrong name for the cell cultures. Therefore, the request asks to replace the name of the cell cultures HTN®Vb with the name EchiPure-PC™ in the designation of the novel food as listed in. Jurisdiction: EU Amends: Commission Implementing Regulations (EU) 2017/2470 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the council on novel foods Mini Summary. Novel foods are foods or food ingredients that do not have a significant history of consumption within the EU before 15 th May 1997 in accordance with. Commission Implementing Regulation (EU) 2020/1559 of 26 October 2020 amending Implementing Regulation (EU) 2017/2470 establishing the Union list of novel foods. Lexparency.org. Regulation (EU) 2020/1559 view on EUR-LEX. In force since August 13rd 2018.

Tentamus Labelling | Tentamus

(2) Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (OJ L 351, 30.12.2017, p. 72) 2 Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (OJ L 351, 30.12.2017, p. 72). 3 Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the approximation of the laws of the Member States. Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods, (EU) 2017/2470 C.F.R. § L 351. 2017

Legislation Food Safet

Commission Implementing Regulation (EU) 2020/1559 of 26 October 2020 amending Implementing Regulation (EU) 2017/2470 establishing the Union list of novel foods New! 2 days ago Institution: European Commissio Information on how EU decisions are made, who is involved, who receives funding from the EU budget, and what documents can be consulted. The Commission publishes annually a report on the implementation of the Staff Regulations' prohibition to senior managers to engage in lobbying or advocacy. Share this page: Was this page useful? Yes No. Is there an issue with this page? European.

Commission Regulation (EU) 2017/2400 of 12 December 2017 implementing Regulation (EC) No 595/2009 of the European Parliament and of the Council as regards the determination of the CO2 emissions and fuel consumption of heavy-duty vehicles and amending Directive 2007/46/EC of the European Parliament and of the Council and Commission Regulation (EU) No 582/2011 (Text with EEA relevance Where AIFMs are exposed to a securitisation that no longer meets the requirements provided for in Regulation (EU) 2017/2402 of the European Parliament and of the Council (*), they shall, in the best interest of the investors in the relevant AIFs, act and take corrective action, if appropriate. STS - Simple - Transparent - Standardized. As part of the regulation, the EU is seeking to. Die Verordnung (EU) 2017/745 über Medizinprodukte ist am 25. Mai 2017 in Kraft getreten. Sie wird auch Medical Device Regulation (MDR) oder europäische Medizinprodukte-Verordnung genannt. Sie gilt in den Mitgliedstaaten der Europäischen Union unmittelbar und muss daher nicht in nationales Recht umgesetzt werden. Gleichwohl werden umfängliche Anpassungen des nationalen Medizinprodukterechts. 2 Commission Implementing Regulation (EU) 2017/2470 of 20 December 2017 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 of the European Parliament and of the Council on novel foods (OJ L 351, 30.12.2017, p. 72). 3 Commission Decision 2008/559/EC of 27 June 2008 authorising the placing on the market of allanblackia seed oil as novel food ingredient under. Commission Implementing Regulation (EU) 2020/478 of 1 April 2020 correcting Implementing Regulation (EU) 2017/2470 establishing the Union list of novel foods (Text with EEA relevance) 7 months ago. Institution: European Commission; Type: Regulation of the EU; Published: OJEU L 102, 02 April 2020 p. 1 7 months ago; Official OJEU page ; 2020; April 2020; 02 April 2020; 2020/L 102; Regulation of.

Regulatory framework. Regulation 2017/2469 on administrative and scientific requirements for novel foods applications Regulation 2017/2468 on administrative and scientific requirements concerning traditional foods from third countries; Regulation 2017/2470 on establishing the Union list of novel food Council Regulation (EU) 2017/1970 of 27 October 2017 Fixing for 2018 the fishing opportunities for certain fish stocks and groups of fish stocks applicable in the Baltic Sea and amending Regulation (EU) 2017/12 Administrative adjustments are made to update the Annex in Regulation (EU) No. 2017/2470 establishing the Union list of novel foods in accordance with Regulation (EU) No. 2015/2283 on novel foods, to include reference for the authorisation of Yarrowia lipolytica yeast biomass * to be placed on the market as a novel food. This sets out the recommended maximum levels on how much Yarrowia. Securitisation - Regulation 2017/2402; Law Securitisation - Regulation 2017/2402. Law details. Information about Regulation 2017/2402 on securitisation. Amending and supplementary acts . Implementing and delegated acts. Related information: Securitisation. Share this page: Was this page useful? Yes No. Is there an issue with this page? European Commission website This site is managed by the.

Durchführungs­verordnung (EU) 2017/2470 - BEHR'SONLIN

Regulations on 12th August 2018 ammend the Commission Implementing Regulations (EU) 2017/2470 establishing the Union list of novel foods in accordance with Regulation (EU) 2015/2283 o the European Parliament and of the council on novel foods. This Regulation replaces the Annex of Regulation (EU) 2017/2470 in order to consolidate amendments which have added authorised novel foods to the Union. Regulation (EU) 2017/745 The European Union Medical Device Regulation of 2017 If you are a manufacturer, authorised representative, importer or distributor of medical devices in the EU, or a regulatory affairs or quality management professional involved with medical devices, you need to know how to comply

EU Amending Implementing Regulation (EU) 2017/2470_Food

  1. Commission Implementing Regulation (EU) 2020/1634 of 4 November 2020 authorising the placing on the market of sugars obtained from cocoa (Theobroma cacao L.) pulp as a novel food under Regulation (EU) 2015/2283 of the European Parliament and of the Council and amending Commission Implementing Regulation (EU) 2017/2470 (Text with EEA relevance) New
  2. EU legislation is divided into primary and secondary. The treaties (primary legislation) are the basis or ground rules for all EU action. Secondary legislation - which includes regulations, directives and decisions - are derived from the principles and objectives set out in the treaties
  3. This Regulation replaces the Annex of Regulation (EU) 2017/2470 in order to consolidate amendments which have added authorised novel foods to the Union list and correct numerous technical errors such as typographic errors. Link to full government text . The Legislation Update Service is the best way to stay up to date automatically with legislation in England, Wales, Scotland, Northern Ireland.
  4. Common principles on granting exemptions under Art. 2(2) of Commission Implementing Regulation EU 2017/2177' Downloads. Croatian translation (pdf, 215.3 KB) Hungarian translation (pdf, 201.33 KB) Finnish translation (pdf, 325.15 KB) Slovak translation (pdf, 365.14 KB) Slovenian Translation (pdf, 750.95 KB) Czech translation (pdf, 576.11 KB) Polish translation (pdf, 327.11 KB) Romanian.
  5. EU legislation takes the form of: Treaties establishing the European Union and governing the way it works; EU regulations, directives and decisions - with a direct or indirect effect on EU member states. Legislation in force. EU law (EUR-Lex) Search for directives, regulations, decisions, international agreements and other act
  6. (1) Regulation (EU) 2015/2283 provides that only novel foods author ised and included in the Union list may be placed on the market within the Union. (2) Pursuant to Ar ticle 8 of Regulation (EU) 2015/2283, Commission Implementing Regulation (EU) 2017/2470 (2
  7. Regulation (EU) 2019/1148 of the European Parliament and of the Council of 20 June 2019 on the marketing and use of explosives precursors, amending Regulation (EC) No 1907/2006 and repealing Regulation (EU) No 98/2013 (Text with EEA relevance). REACH Initial text. Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration.

Related EU legislation. Commission Regulation (EC) No 1234/2008 ('the Variations Regulation') 'Variations guidelines' - Guidelines on the details of the various categories of variations, on the operation of the procedures laid down in Chapters II, IIa, III and IV of Commission Regulation (EC) No 1234/2008 of 24 November 2008 concerning the examination of variations to the terms of marketing. Regulation (EU) 2018/1139 of the European Parliament and of the Council of 4 July 2018 on common rules in the field of civil aviation and establishing a European Union Aviation Safety Agency, and amending Regulations (EC) No 2111/2005, (EC) No 1008/2008, (EU) No 996/2010, (EU) No 376/2014 and Directives 2014/30/EU and 2014/53/EU of the European Parliament and of the Council, and repealing.

Juni 2017 wurde die Verordnung (EU) 2017/989 zur Änderung der Durchführungsverordnung (EU) zum Unionszollkodex 2015/2447 (Implementing Act, UZK-IA) im Amtsblatt Nr. L 149 Änderungen zum UZK-IA veröffentlicht. Sie tritt am 14. Juni 2017 in Kraft. Neben der Anpassung verschiedener IA-Artikel wurde insbesondere auch Art. 62 UZK-IA zur Langzeit-Lieferantenerklärung neu formuliert. Die EU. Regulation (EU) 2017/745 is a regulation of the European Union on the clinical investigation and sale of medical devices for human use. It repeals Directive 93/42/EEC, which concerns medical devices, and Directive 90/385/EEC, which concerns active implantable medical devices, on 26 May 2021.. The regulation was published on 5 May 2017 and came into force on 25 May 2017

Novel food Food Safety - European Commissio

  1. Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (General Data Protection Regulation) (Text with EEA relevance
  2. ary discussions of the Commission services and Member States' authorities, and they may not.
  3. Do you want to publish EU funding opportunities on your website? Call now: +34 91 119 69 77. Euroalert Newsletters Subscribe now to receive funding opportunities instantlly. Want another formats? Call now: +34 91 119 69 77. COMING SOON: Euroalert 10ders. is about making public procurement made easy for SMEs . Want to receive alerts on public sector contracts? Want to make better decissions.

In July 2017, the SEC released an investigative report that highlighted that such tokens can be subject to the full scope of US securities regulation. As a result, issuers increasingly structure ICOs such as to prevent US citizens and residents from obtaining tokens in order to exclude the reach of US securities regulation. However, for the time being, EU citizens and residents are free to. REGULATION (EU) 2017/1369 for energy labelling valid from 1 August 2017 On 28 July 2017, this Regulation was published and has been valid since 1 August 2017. As a framework regulation, the regulation sets the benchmarks for the product regulations, e.g. 874/2012 for lamps and luminaries. The special feature of this framework regulation

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. ) DisplayLogo. Publications Office of the European Union. MainSearch. search. More Advanced search Browse by. 2017-07-06: Ergebnisse des BVmed-Rechtssymposiums: Durch MDR steigen Kosten und Aufwand (nicht überraschend) 2017-05-05: Die MDR ist im Amtsblatt erschienen. Damit tritt die Medical Device Regulation am 25. Mai 2017 in Kraft und wird gültig am 26. Mai 2020. 2017-04-04: Das EU-Parlament verabschiedet die MD

April Jahr 2017 (EU-Amtsblatt Nr. L 117, S. 1 und S. 176 vom 5. 5. 2017) und können bereits seit November 2017 im Übergang von dem alten zu dem neuen Recht angewendet werden. Endgültig gelten. Mehr Transparenz und mehr Anlegerschutz. Zu den prägenden Themen des Jahres 2017 gehörte die Umsetzung der MiFID II, die zweite europäische Finanzmarktrichtlinie (Markets in Financial Instruments Directive). 1 Deren Regelungen gelten seit dem 3. Januar 2018. Ziel der Novelle ist es, die Funktionsweise und Transparenz der Finanzmärkte zu verbessern und Verbraucher in der Europäischen Union. COMMISSION IMPLEMENTING REGUL ATION (EU) 2017/94 of 19 Januar y 2017 imposing a def initive anti-dumping duty on impor ts of sodium gluconate or iginating in the People's Republic of China following an expir y review pursuant to Ar ticle 11(2) of Regulation (EU) 2016/1036 of the European Parliament and of the Council THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of. REGULATION (EU) 2017/2321 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 12 December 2017 amending Regulation (EU) 2016/1036 on protection against dumped imports from countries not members of the European Union and Regulation (EU) 2016/1037 on protection against subsidised imports from countries not members of the European Union . This is a redirection page. The requested document has been.

BEREC Guidelines on Regulation (EU) No 531/2012, as amended by Regulation (EU) 2015/2120 and by Regulation (EU) 2017/920 (Wholesale Roaming Guidelines) Document number: BoR (17) 114 Document date: 09.06.2017 Date of registration: 09.06.2017 Document type: Guidelines Author: BEREC. These Wholesale Roaming Guidelines replace the BEREC Guidelines of 2012 (BoR (12) 107) which concern the wholesale. March 2019 supplementing Regulation (EU) 2017/1129 of the European Parliament and of the Council as regards the format, content, scrutiny and approval of the prospectus to be published when securities are offered to the public or admitted to trading on a regulated market, and repealing Commission Regulation (EC) No 809/2004 2 1 OJ L 166, 21.06.2019, p. 1-25 2 OJ L 166, 21.06.2019, p. 26-176.

Foodlaw-Reading - EU Food Laws 2017

Updates to Novel Food - Regulation (EU) 2015/2283 and

Regulation (EU) 2020/1559 - lexparency

  1. Die EU-Mitgliedstaaten haben die Zulassung des umstrittenen Unkrautvernichters Glyphosat um fünf Jahre verlängert. 18 der 28 EU-Länder stimmten für einen entsprechenden Vorschlag der EU.
  2. Mai 2017) im EU-Amtsblatt gemeinsam mit der IVD-Verordnung bekannt gemacht worden. Darauf hat der Bundesverband Medizintechnologie, BVMed, hingewiesen. Offizielles Inkrafttreten der europäischen Verordnungen ist 20 Tage nach der Veröffentlichung, also am 25. Mai 2017. Die MDR ist dann nach einer dreijährigen Übergangszeit ab 26. Mai 2020 verpflichtend anzuwenden. Nach Ansicht des BVMed ist.
  3. Die EU-Institutionen erhalten mehr Zeit (bis zum 1. Januar 2019), um sich - sofern ihre Verwaltungsausgaben betroffen sind - an die neuen Vorschriften anzupassen. Omnibus-Verordnung (Volltext) Vereinfachte Vorschriften für die Verwendung von EU-Mitteln: Rat bestätigt Einigung mit dem Parlament (Pressemitteilung, 19. April 2018
  4. Die EU-Medizinprodukte-Verordnung (Medical Device Regulation = MDR) wurde am 5. April 2017 vom Europäischen Parlament verabschiedet - diese Nachricht dürfte sich inzwischen entsprechend verbreitet haben, sodass Sie die ersten Zeilen mit einem leichten Schulterzucken wahrnehmen und denken werden: Das ist inzwischen bekannt, was jetzt? Nun - beginnen wir doch mit den nackten Zahlen: Im.

The Amending Regulation contains a number of provisions that will apply as and from 1 October 2017, as they had to be developed by secondary legislation. The secondary legislation consists of the Delegated Regulation (EU) 2018/625 supplementing Regulation (EU) 2017/1001 and the Implementing Regulation (EU) 2018/626 laying down detailed rules for implementing certain provisions of Regulation. Die Verwendung fluorierter Treibhausgase ist seit 2006 in der Verordnung (EG) Nr. 842/2006 und in der Richtlinie 2006/40/EG geregelt. Seit 1. Januar 2015 gilt die Verordnung (EU) Nr. 517/2014 über fluorierte Treibhausgase. Damit ist die Verordnung (EG) Nr. 842/2006 aufgehoben See also. Staff regulations; Eur-Lex. Eur-Lex:52019DC0617: Report from the Commission to the European Parliament and the Council on data pertaining to the budgetary impact of the 2019 annual update of remuneration and pensions of the officials and other servants of the European Union and the correction coefficients applied thereto.COM/2019/617 final, 28.11.201 Verordnung (EU) Nr. 2017/1001 im Vergleich zu Verordnung (EG) Nr. 207/2009 (einschließlich Änderungen) Übergangsvorschriften (UMDV, DVUM) Reform der unionsmarke - Zusammenfassung der Änderungen, die am 1.Oktober 2017 in Kraft trete Die neue EU-Medizinprodukteverordnung (MDR) ersetzt die aktuelle Medizinprodukterichtlinie (93/42/EWG) sowie die Richtlinie über aktive implantierbare medizinische Geräte (90/385/EWG). Die Verordnung über Medizinprodukte (Medical Device Regulation, MDR) wurde am 5. Mai 2017 veröffentlicht und trat am 25. Mai 2017 in Kraft. Für Hersteller.

The EU general data protection regulation 2016/679 (GDPR) will take effect in May 25 2018. Regrettably Brussels does not deliver an easy readable text for 99 articles and 173 recitals. We fill in this blank (with table of contents, hyperlinks, markups, with correction and dossier-functionality). All this is part of our PrivazyPlan® April 2017 seinen Standpunkt fest, der an die EU-Botschafter im AStV weitergeleitet wurde. Der AStV verständigte sich am 28. Juni 2017 auf ein Verhandlungsmandat des Rates für die gesamte vorgeschlagene Omnibus-Verordnung und gab dem Vorsitz grünes Licht, die Verhandlungen mit dem Europäischen Parlament aufzunehmen The MDR will replace the EU's current Medical Device Directive (93/42/EEC) and the EU's Directive on active implantable medical devices (90/385/EEC). The Medical Device Regulation was officially published on May 5th 2017 and came into force on May 25th 2017 REGULATION (EU) 2017/2226 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 30 November 2017 establishing an Entry/Exit System (EES) to register entry and exit data and refusal of entry data of third-country nationals crossing the external borders of the Member States and determining the conditions for access to the EES for law enforcement purposes, and amending the Convention implementing the. Regulation (EU) 2017/1129 of the European Parliament and of the Council of 14 June 2017 on the prospectus to be published when securities are offered to the public or admitted to trading on a regulated market, and repealing Directive 2003/71/EC3 Abbreviations ESMA European Securities and Markets Authority RD Registration Document Definitions Persons responsible for the prospectus The persons.

Commission Implementing Regulation (EU) 2020/1559 of 26

Mythocondro® is now registered in the Union List of Novel

Fee Regulation. Commission Regulation (EU) 440/2010 of 21 May 2010 on the fees payable to the European Chemicals Agency pursuant to Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures. Further information . Further information related to the background and development of the CLP Regulation may be found. Directive (EU) 2016/97 of the European Parliament and of the Council of 20 January 2016 on insurance distribution (IDD), Commission Delegated Regulations supplementing Directive (EU) 2016/97, Commission Implementing Regulation (EU) 2017/1469 and EIOPA Guidelines under Directive (EU) 2016/9 Legislation and case-law . Find legislation ; Find case-law ; Have your say . Get involved in European policy making This page contains visual material - slide presentations - illustrating various aspects of the EU. These slides may be a useful tool for teachers, speakers on EU issues, students and anyone interested in giving a presentation about the EU. They offer clear explanations on. Die EU-DSVGO, auch General Data Protection Regulation (GDPR) genannt, wurde bereits 2016 von der EU beschlossen und soll eine einheitliche Richtlinie bieten für den Schutz von privaten und personenbezogenen Daten. Davon betroffen sind Unternehmen und auch öffentliche Institutionen die personenbezogene Daten speichern oder auch verarbeiten. Es gibt keine Ausnahmen für Firmen von.

PQQ Disodium Salt approved by EC as novel foods | Herb

Die Medical Device Regulation (MDR), Europäische Verordnung für Medizinprodukte, trat gemeinsam mit der Verordnung für In-vitro-Diagnostika (IVDR) am 25.Mai 2017 offiziell in Kraft. Die MDR ist nach einer vierjährigen Übergangszeit ab 26. Mai 2021 verpflichtend anzuwenden. EU-Verordnung für Medizinprodukte (PDF 1,6 MB Vaccine regulation National regulatory authorities. The assessment, licensure, control, and surveillance of biological medicinal products are major challenges for national regulatory authorities confronted by a steadily increasing number of novel products, complex quality concerns, and new technical issues arising from rapid scientific advances Die neue europäische Verordnung (EU) 2016/425 über persönliche Schutzausrüstungen (PSA) wurde am 31. März 2016 im Amtsblatt der Europäischen Union veröffentlicht und ist nach einer Vorlaufzeit von zwei Jahren ab dem 21. April 2018 verbindlich anzuwenden. Zu diesem Zeitpunkt ersetzt die neue PSA-Verordnung die bisherige Richtlinie 89/686/EWG pollutant emission limits and type-approval for internal combustion engines for non-road mobile machinery, amending Regulations (EU) No 1024/2012 and (EU) No 167/2013, and amending and repealing Directive 97/68/EC . was published in the Official Journal of the EU on 16September 2016 and entered into force on 6 October 2016. The regulation shall apply from 1 January 2017. Directive 97/68/EC is.

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