Processo de designação para o IVDR – Regulation (EU) 2017/746 dos membros do Team-NB
http://www.team-nb.org/team-nb-publishes-a-press-release-regarding-the-designation-process-in-the-framework-of-the-ivdr-regulation/
Team-NB publishes a press release regarding the designation process in the framework of the IVDR regulation – Regulation (EU) 2017/746
Published in In Vitro Diagnostic Medical Devices Directive - IVDMDD and Team-NB
More from In Vitro Diagnostic Medical Devices Directive - IVDMDDMore posts in In Vitro Diagnostic Medical Devices Directive - IVDMDD »
- EU – Commission Implementing Regulation (EU) 2020/666 of 18 May 2020 amending Implementing Regulation (EU) No 920/2013 as regards the renewal of designations and the surveillance and monitoring of notified bodies
- EU – Manufacturer incident report 2020
- EU – Guidance on temporary extraordinary measures related to medical device Notified Body audits during COVID-19 quarantine orders and travel restrictions
- EU – Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context
- Joint Action on Market Surveillance of Medical Devices (JAMS) Stakeholder Conference Held In Brussels On Dec. 12th 2019
More from Team-NBMore posts in Team-NB »
- EU – Team NB position statement on the requirements for the EU MDR/IVDR Notified Body Partners under the Technical Cooperation Program on Exchange of Medical Device Quality Management System Regulation and ISO 13485 Audit Reports (TCP III)
- EU – Team-NB – Contacts to allow the check of the validity of the CE certificates
- EU – Team-NB Position Paper on Documentation Requirements for Drug Device Combination Products Falling in the Scope of Article 117 of MDR 2017/745.
- EU – Team-NB-Position paper on Dental Implants-20200311-V1
- Team-NB published a press release regarding the survey run among its members to analyse the certificates being issued
Be First to Comment