Responsible persons for promotion of medicinal products in France, Germany, Spain, Italy and United Kingdom

May 28, 2021
  • Promotional Material Review


The promotion of medicinal products is governed by different regulations and codes in the European Union (EU). In particular, the Directive 2001/83/EC ‘of the European parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use’ establishes the European regulatory framework with articles dedicated to promotion activities and advertising of medicinal products.

Register to download the White paper

    By sending this form, I agree that my personal data will be saved and processed according to data protection regulations and will be used only for commercial and marketing purposes only.

    Learn more

    BlueReg undertakes to comply with the regulations in force applicable to the processing of personal data and, in particular, Regulation (EU) 2016/679 of the European Parliament and of the Council of 27 April 2016 applicable as from 25 May 2018 (hereinafter, "the General Data Protection Regulations" or GPDR) and the national laws resulting therefrom.
    Any inquiries, correction or declaration of event related to personal data processed should be sent to: GDPR data request

    GDPR data request

    Thank you for your interest in BlueReg

    The file will be sent to you by email.

    Download your White paper

    Line - Organism