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
