Supporting a biopharmaceutical company not established in Europe accessing SME incentives granted by the European Medicines Agency

May 3, 2022
  • Drug Development

A US‑based client entrusted the European legal representation and the application/granting of their SME status to BlueReg.

BlueReg coordinated the client’s SME dossier preparation and submission to EMA, optimising the application content to expedite its approval.

Register to 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