DLRC Pharma Services

We help non-EU pharmaceutical companies to meet EU pharmaceutical legislation with a range of regulatory representative services

Helping non-EU companies meet EU pharmaceutical legislation

EU pharmaceutical legislation requires that Sponsors are established in the EU/EEA in order to conduct specific activities (e.g. clinical trials), act as an applicant/holder for Orphan Drug Designations and Marketing Authorisations or to access SME benefits.

These requirements can be problematic for non-European sponsors, especially small biotechs or start-ups. To help you access and navigate the EU regulatory system, DLRC Pharma Services provide a full range of EU representative services.

DLRC Pharma Services is a member of the DLRC Group of companies. DLRC has been providing regulatory services since 2005 and our consultants have over 600 years of collective regulatory experience

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