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All NewsPascalePerspectives2024-03-05T14:08:18+01:00

February 2020

62nd NB-Med meeting is planned on April 1st and 2nd in Brussels.

62nd NB-Med meeting is planned on April 1st and 2nd in Brussels.

General Assembly of the association will take place at the Hotel Martin’s Brussels EU.

General Assembly of the association will take place at the Hotel Martin’s Brussels EU.

January 2020

From February 1st 2020, the Withdrawal Agreement provides for a transition period until 31 December 2020 during which Union law continues to apply to and in the UK.

From February 1st 2020, the Withdrawal Agreement provides for a transition period until 31 December 2020 during which Union law continues to apply to and in the UK.

European Commission makes a call for Medical Device Experts on Specific Topics

European Commission makes a call for Medical Device Experts on Specific Topics

Call for experts on medical devices and in vitro diagnostic [...]

December 2019

The Joint Action on Market Surveillance group held a conference opened to all stakeholders with the aim to present to the audience the key deliverables and outputs of the Joint Action.

The Joint Action on Market Surveillance group held a conference opened to all stakeholders with the aim to present to the audience the key deliverables and outputs of the Joint Action.

Euromcontact invited Team-NB to speak at their Regulatory Affairs group meeting to cover items such as designations of notified bodies, difficulty of small businesses in finding a notified body, interpretation of Rule 21, Annex XVI and questions on labelling

Euromcontact invited Team-NB to speak at their Regulatory Affairs group meeting to cover items such as designations of notified bodies, difficulty of small businesses in finding a notified body, interpretation of Rule 21, Annex XVI and questions on labelling

MRA with Switzerland. As long as the agreement is not signed, the MDR/IVDR Notified bodies must request an authorized representative for Swiss Manufacturers when applying for the MDR/IVDR.

MRA with Switzerland. As long as the agreement is not signed, the MDR/IVDR Notified bodies must request an authorized representative for Swiss Manufacturers when applying for the MDR/IVDR.

November 2019

Call for Experts on Medical Devices and In-vitro Diagnostic Medical Devices – EXTENDED

Call for Experts on Medical Devices and In-vitro Diagnostic Medical Devices – EXTENDED

The European Commission has extended the call for expression of [...]

October 2019

New member

New member

Team-NB welcomes a new member from Belgium : SGS (NB [...]

September 2019

Extraordinary General Assembly of the association will take place in Brussels, at the Bedford Hotel & Congress Centre

Extraordinary General Assembly of the association will take place in Brussels, at the Bedford Hotel & Congress Centre