• Advocacy work for medtech and pharma industries
      Acting with a global mindset, MPP’s initial focus will be on the upcoming implementing and delegated acts of the new Medical Devices and in vitro Diagnostics Regulations (MDR / IVDR) as well as amendments to the Medicinal Product Directive 2001/83 affecting combined products

    • MPP expert trainings and scientific knowledge base
      Specialized, accredited training courses providing comprehensive and up-to-date insights on latest developments of legislation

    • MPP annual conference
      Industry and stakeholders platform to discuss trends, opportunities and industry challenges