A minor matter quickly dealt with.
Welcome to LegalRep UG - Effortless compliance with Article 74 of the EU Trial Regulations.
Our service consists of meeting the exact requirements of Article 74 without unnecessary complexity.
Our Approach:
Clear Guidance: We offer the service you truly need
Minimalism: No unnecessary extras, just what the law demands
Bureaucracy-Free: Effortless compliance, hassle-free experience.
We adhere to what the law prescribes, nothing more. In this way, we simplify your path to compliance
By doing just this, we are the perfect partner for orphan drug designation holders and for small and medium enterprises.
Ready to uncomplicate your EU clinical trials?
WANT TO BENEFIT FROM EMA STATUS AS MICRO, SMALL AND MEDIUM ENTERPRISE? WE CAN
HELP. JUST CONTACT US
WANT TO CONDUCT A CLINICAL TRIAL IN THE EU BUT HAVE NO LEGAL ENTITY THERE? WE CAN HELP.
WANT TO GET ORPHAN DRUG DESIGNATION IN THE EU FOR YOUR INNOVATIVE MEDICINAL
PRODUCT BUT HAVE NO LEGAL ENTITY THERE? WE CAN HELP. JUST CONTACT US
Who we are
LegalRep UG was founded in August 2016 with the purpose of providing the services as legal representative in the European Union for pharmaceutical companies that have no legal entity within the EU.
With our service as legal representative, there will be no need for non-EU pharmaceutical companies
to establish an affiliate in the EU.