272 (7) If the name of a person is removed from a list by a manager or by the authorised representative the registration of that person as a designated representative is cancelled and the person may not act as a designated representative or be included on any list a copy of which is submitted under section 182 for such period as NAMFISA may determine.

Booking Software by Rezdy.com | Agent login. Finder AU We are also a Corporate Authorised Representative of Countrywide Insurance Group Pty Limited.

An authorized representative assumes responsibility for compliance with the quality and safety standards; On the basis of a service contract with the manufacturer, the authorized representative carries out the conformity confirmation of the products with the requirements of the technical regulation in his own name and responsibility. 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. Section 116 provides qualification, disqualification and other procedures relating to the authorized representative which are articulated under this article for the goods and service tax. As your Authorised Representative, we will provide you with our name and contact details, to place on the product, it's packaging or accompanying documentation. Scope of Service Our service will apply to the following regulations and directives ( however, this is not the exhaustive list of directives which regulation 2019/1020 applies to, for full list please go to article 4.5 of the Regulation ) Schedule C – Authorised Representative Authority.

An authorised signatory from the submitting entity will need to delegate Register the company and add your name as a company representative. You will then Medical Products Agency hereby confirms that the above mentioned manufacturer/authorised representative has registered the listed medical LVFS 2001:5 on active implantable medical devices. The manufacturer or his authorised representative is responsible for the products listed in Certificate of registration / Registreringsbevis. Manufacturer or Authorised Representative / Tillverkare eller Auktoriserad Representant.

We may appoint other Authorised Representatives or Corporate Authorised Representatives, on the same or different terms. CAR Representative's Appointment.

authorised representative. The obligations laid down in Article 7(1 ) a nd the obligation to draw up technical documentation referred to in Article 7(2 ) shall not form part of the authorised representative’s mandate. 2.

3 Feb 2021 The deadline of 16 July 2021 will impact products with CE marking: they will now all need an authorised representative in Europe.

APPOINTMENTS. APPOINTMENT. Australian financial services (AFS) licensees can appoint persons or companies as “ Перевод контекст "authorised representative" c английский на русский от Reverso Context: In compliance with legal acts, in order to protect the rights and Your regulatory gateway to Europe Authorized Representative services for in vitro diagnostics(ivd) and medical devices (md). Translations, Consulting Animal name.

Cross endorsements 2020-05-08 · An authorised representative is a natural person with his or her principal place of residence in Singapore. He or she is appointed for the purpose of accepting service of process or any notices required to be served on the Singapore branch of a foreign company.
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The annual fee for the service is 5 000 SEK. The authorised representative shall perform the tasks specified in the mandate agreed between it and the manufacturer. The authorised representative shall provide a copy of the mandate to the competent authority, upon request.

This is why there has to be authorized or appointed a person, who can represent the company in all sorts of matters.
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A European Authorized Representative is a natural or legal person who acts on behalf of the manufacturer in relation to the CE legislation. Regardless of whether

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 Se hela listan på conformance.co.uk The responsibilities of the departing European Authorized Representative after the end of the mandate to forward to the manufacturer or incoming European Authorized Representative regarding any complaints or reports from healthcare professionals and users about suspected incidents or adverse events related to a medical device/IVD for which it had been designated as the EC Rep. Authorised Representative Service EU. 77 Camden Street Lower Dublin D02 XE80 Ireland. Tel: +353 1903 6214. Authorised Representative Service UK. Great Hucklow Buxton Derbyshire SK17 8RG United Kingdom. Tel: +44 (0)1298 873837.