Global Regulatory Affairs (GRA) Outsourcing Platform

Marketing Communication
Regulatory affairs Pharmaceutical industry
Regulatory affairs Pharmaceutical industry
February 18, 2020
image_pdfPDF

A global biopharmaceutical company entrusted to BlueReg the management of daily regulatory activities for a large portfolio of medicinal products in various therapeutic areas, the objective being to focus their internal resources on strategic projects. The outsourced activities encompassed development and post-authorisation regulatory activities (including publishing services) for Europe in addition to selected activities for intercontinental regions for a large portfolio of medicinal products.

Download the
Case Study

    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 Case study