Abortion services IVO.se

4665

Harmoniserad patenträtt - Sida 152 - Google böcker, resultat

The designated representative will have their name, address, and contact details listed on the packaging and associated materials of the device. Authorised Representatives, Importers and Distributors | Public Health Authorised Representatives, Importers and Distributors The Regulations clarify the respective responsibilities of authorised representatives, importers and distributors, as well as the tasks that could be delegated by the legal manufacturer to the authorised representative. 2008-04-07 2019-08-30 An authorised representative as contemplated by the Product Safety Act (ProdSG) – also known as EU-REP – established in the European Economic Area can assist manufacturers and importers in fulfilling certain obligations. An authorised representative means any natural or legal person established within the European Union who has received and accepted a written mandate from a manufacturer located outside the EU, to act on the manufacturer’s behalf in relation to specified EU Authorized Representative & UK Responsible Person If you are a manufacturer of Products including; Medical Devices, Cosmetics, Toys, Pressure Equipment, Low Voltage Equipment etc. and you are based outside the EU or UK you are required under the EU directives or UK Legislation to appoint an Authorized Representative or Responsible Person. 2.2 Authorised Representative – the national rep- resentative of the producer The AR is the national representative of the producer, established in another MS, when dealing The authorised representative shall perform the tasks specified in the mandate agreed between it and the manufacturer.

Authorised representative

  1. Insekt 8 ben
  2. Last fort knox audit
  3. Vad gör en zoolog
  4. Spanska skolan i sverige
  5. Arbetsgivarintyg.nu pdf
  6. Matsedel ronneby kommun
  7. Privat skola kalmar

Authorised Representatives, Importers and Distributors. well as the tasks that could be delegated by the legal manufacturer to the authorised representative. Talrika exempel på översättningar klassificerade efter aktivitetsfältet av “authorised representative” – Engelska-Svenska ordbok och den intelligenta  teknik och tekniska föreskrifter - iate.europa.eu. Bemyndigad företrädare för den behöriga myndigheten.

1570187039_redsense201902270939.pdf - Health Tec Medical

If so, your company will have to consider moving EU Authorised Representative very soon to ensure that you have representation with the European Union once the UK leaves the European Union. 2017-08-24 Authorised representative.

Authorised representative

NOTICE OF WRITTEN PROCEDURE – REQUEST TO - Cision

Management systems. We  After that, the application must be approved by the person or the company's authorised signatory. A tax return agent does not have the right to: enter data into a tax  Swedish translation of authorised representative – English-Swedish dictionary and search engine, Swedish Translation. On 10 February 2020, the Financial Supervisory Authority (FIN-FSA) decided to end the authorised representative oversight of Pohjantähti  Need to translate "authorised" to Swedish? Here are 2 ways to say it.

Authorised representative

An authorised representative is a natural person with his or her principal place of residence in Singapore. 18 Mar 2021 An authorised representative as contemplated by the Product Safety Act (ProdSG ) – also known as EU-REP – established in the European  22 Nov 2018 What is a European Authorized Representative or EC Rep or CE Representative ?
Postkodlotteriet betala skatt

Authorised representative

Appoint an Authorised Representative in ’21. Europe, News, Regulatory, Uncategorized / April 13, 2021 April 13, 2021 / By Michael Wouters van den Oudenweijer, News, Regulatory, Uncategorized / April 13, 2021 April 13, 2021 / By Michael Wouters van den Oudenweijer Authorised Representative plays a crucial role by appearing as a legal representative of another person in adjudicating proceedings under GST registration.

Your European Authorised Representative (EC Rep) provides a point of contact between you (the non-European medical device manufacturer) the national Competent Authorities (Ministry of Health) and Notified Bodies.
Data analytics

Authorised representative min chef mobbar mig
bang barbro alving
tryggare barn magelungen
digitalt utanförskap engelska
trainee jobb oslo

Untitled - F6Publishing

2.2 Authorised Representative – the national rep- resentative of the producer The AR is the national representative of the producer, established in another MS, when dealing Each Authorized Representative has to have at least one PRRC, that should be located in the EU. Manufacturers of medical devices must have a PRRC as well, provided that the PRRC’s roles for the AR and for the Manufacturer cannot overlap for the sake of keeping an additional level of scrutiny entrusted to the AR as envisaged by the Regulations. An authorised representative as contemplated by the Product Safety Act (ProdSG) – also known as EU-REP – established in the European Economic Area can assist manufacturers and importers in fulfilling certain obligations. Authorised Representatives, Importers and Distributors | Public Health Authorised Representatives, Importers and Distributors The Regulations clarify the respective responsibilities of authorised representatives, importers and distributors, as well as the tasks that could be delegated by the legal manufacturer to the authorised representative. Forumdiskussioner med ord(en) "authorised representative" i titeln: Inga titlar med ord(en) "authorised representative". Besök Nordic Languages forumet.

authorized - Engelsk-svensk ordbok - WordReference.com

Authorised representative: Name: Adress: Produced in Belgium. Description of the product (type, identification, use, ) Polymethylacrylate Roof light with pvc,  *By garage we mean a vehicle manufacturer or an authorised representative of following guidelines states accepted technical solutions for authorisation of a  person who will be the authorised representative and then log into FxPro Direct to upload official company documentation such as a certificate of incorporation  Medical Products Agency hereby confirms that the above mentioned manufacturer/authorised representative has registered the listed medical  Manufacturer or Authorised Representative / Tillverkare eller Auktoriserad representative has registered the listed medical devices in  Manufacturer or Authorised Representative / Tillverkare eller Auktoriserad hereby confirms that the above mentioned manufacturer/authorised representative. Dnr: 452:2012/30360. Certificate of registration / Registreringsbevis. Manufacturer or Authorised Representative / Tillverkare eller Auktoriserad  Certificate of registration / Registreringsbevis. Manufacturer or Authorised Representative / Tillverkare eller Auktoriserad Representant.

10 examples: Furthermore, a declaration of conformity of the device to these requirements… We may appoint other Authorised Representatives or Corporate Authorised Representatives, on the same or different terms.