A leading global medical devices manufacturer requested Cambre’s support to positively profile themselves towards EU policy-makers and stakeholders, in the context of the revision of the new EU medical devices legislation.
A leading global medical devices manufacturer requested Cambre’s support to build their profile towards EU decision-makers; to enhance their corporate reputation in Brussels; and directly engage with EU politicians and officials to support an optimal outcome of the new medical devices legislation.
Cambre proposed an integrated approach to (1) rapidly build the company’s Brussels network, (2) raise its profile within relevant trade associations, (3) position Government Relations within its business, and (4) build its Public Affairs capability. Cambre currently provides the company with strategic counsel and intelligence-gathering on an ongoing basis, and is integral to the company’s broader Brussels advocacy and communications work.
Cambre is building the company’s reputation and is supporting the development of ‘thought leadership’ positions on corporate issues and in key therapeutic areas. The company is well positioned to influence new legislation and is actively engaged in discussions with Members of the European Parliament, EU Member State representatives and EU officials.