• Inicio
  • Formações
  • Formação à Medida
  • News & Trends
  • Sobre nós
  • Contacto

Register as a manufacturer to sell medical devices from 1 January 2021

 

Published 7 December 2020
Last updated 7 December 2020 — see all updates
From:
Medicines and Healthcare products Regulatory Agency
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland from 1 January 2021

Contents

  1. Overview
  2. Who must register
  3. When you must register
  4. Information required when registering your devices with the MHRA
  5. Apply to register on the Device Online Registration System (DORS)
  6. Fees
  7. Making changes to your registration
  8. Public register of manufacturers
  9. Reference guides
  10. Contact

 

News & Trends

Procurar

Recentes

  • Digital label for authorised representative and importer
  • MANUAL PARA REGULARIZAÇÃO DE EQUIPAMENTO MÉDICO E SOFTWARE COMO DISPOSITIVO MÉDICO NA ANVISA
  • How to Prepare a PreRequest for Designation (Pre-RFD) . FDA Guidance for Industry
  • Formação exclusiva Formiventos CTD MODULO 3: “Evento de alta qualidade que permitiu grande interação entre todos os participantes. “
  • PREÇOS 2025: “Muito interessante e enriquecedora”
  • GUIDANCE DOCUMENT Alternative Tools: Assessing Drug Manufacturing Facilities Identified in Pending Applications
  • FDA Releases Draft Guidance on Quality Management System (QMS) Requirements for Premarket Submissions (October 2025
  • FARMACOVIGILÂNCIA avançada: ““Excelente! Organizada e abrangente !”

91 257 00 03 (Chamada para a rede móvel nacional)
info@formiventos.com

  • Follow
  • CLIENTES & TESTIMONIALS
  • ASSOCIAÇÕES OFICIAIS
  • CERTIFICAÇÕES E CREDITAÇÕES
  • ADVISORY BOARD
  • Política de Privacidade
  • Contacto