MedTech in France

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2022
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No longer registered as of 24 Nov 2022 - Registration as it was on 22 Aug 2022
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Overview

Lobbying Costs

10,000€ - 24,999€

Financial year: Jan 2021 - Dec 2021

Lobbyists (Full time equivalent)

1 Fte (3)

Lobbyists with EP accreditation

0

High-level Commission meetings

1

Lobbying Costs over the years

  • Info

    MedTech in France

    EU Transparency Register

    229391544746-22 First registered on 23 Nov 2021

    Goals / Remit

    Created in 2013, the MedTech in France association's mission is to help French medical technology champions emerge. It brings together some 40 of the best French MedTechs, from e-health to surgical robotics, telemedicine, optical technologies, wound healing and medical imaging.

    Its members are entrepreneurs with production or research and development activities in France. They all share the observation that the medical technology sector has a strong potential for innovation. It therefore seemed necessary to them to put together a coordinated approach to promote its development.

    MedTech in France is open to companies directly involved in the design, production or delivery of devices or services in the medical technology industry, as well as to players who can contribute to the development of the sector. Members meet several times a year in Paris.

    Main EU files targeted

    * MDR
    * Implementation of Regulation (EU) 2017/746 on in vitro diagnostic medical devices and Regulation (EU) 2017/745 on medical devices
    * Blood, tissues and cells legislation
    * Implementation of the late payments directive
    * Policies, Initiatives related to Antimicrobial Resistance (AMR) and Healthcare-Associated Infections (HAIs)
    * EU Health Technology Assessment
    * Cross-Border Health Care
    * Health system performance assessments / EU semester
    * Environmental regulations and their implementation (e.g., The WEEE and RoHS Directives, and the REACH, POPs and Biocidal Products Regulations)
    * The European Green Deal
    * Corporate Social Responsibility
    * General Product Safety Directive
    * Patient safety and quality of care
    * EU Directive on Procurement
    * Public Procurement of Innovation Solutions
    * Research Framework Program
    * Public Private Partnership in Healthcare
    * E-privacy, Digital Single Market initiatives
    * Digital transformation of health and care
    * The European Health Data Space
    * Artificial intelligence
    *Product Liability

    Address

    Head Office
    15 avenue de Iéna
    PARIS 75016
    FRANCE
    EU Office
    15 avenue de Iéna
    PARIS 75016
    FRANCE

    Website

  • People

    Total lobbyists declared

    3

    Employment timeLobbyists
    50%1
    25%2

    Lobbyists (Full time equivalent)

    1

    Lobbyists with EP accreditation

    No lobbyists with EP accreditations

    Complementary Information

    None declared

    Person in charge of EU relations

    Data not provided by Register Secretariat due to GDPR

    Person with legal responsibility

    Data not provided by Register Secretariat due to GDPR

  • Categories

    Category

    Trade unions and professional associations

  • Networking

    Affiliation

    Not applicable

    Member organisations

    None declared

  • Financial Data

    Interests represented

    Promotes their own interests or the collective interests of their members

    Closed financial year

    Jan 2021 - Dec 2021

    Lobbying costs for closed financial year

    10,000€ - 24,999€

    Major contributions in closed year

    None declared

    Intermediaries for closed year

    None declared

    Intermediaries for current year

    Name
    brunswick group

    Closed year Costs

    10,000€ - 24,999€

    Other financial info

    None declared

  • EU Structures

    Groups (European Commission)

    none

    Groups (European Parliament)

    N/A

    Communication activities

    Not applicable

    Other activities

    None declared

  • Meetings

    Meetings

    1 meetings found. Download meetings

    The list below only covers meetings held since November 2014 with commissioners, their cabinet members or directors-general at the European Commission; other lobby meetings with lower-level staff may have taken place, but the European Commission doesn't proactively publish information about these meetings. For more information about which commissioner is responsible for which portfolio, check out this link: https://commissioners.ec.europa.eu/index_en All information below comes from European Commission web pages.

    • Date 26 Jan 2022 Location Brussels, Belgium
      Subject Strategic autonomy of the health industrial ecosystem, in particular the medical device sector
      Cabinet Cabinet of Commissioner Thierry Breton
      Portfolio Internal Market
      Attending
      • Maurits-Jan Prinz (Cabinet member)
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