The leading experts in EU Representation and Regulatory Affairs for pharmaceutical and biotechnology in a Brexit environment.

The strategic location of IDEA’s London and Dublin offices means we can offer an unparalleled, simple, and speedy service to UK sponsors running EU clinical trials who need an EU legal representative quickly. Contact our experts to ensure you will remain compliant post-Brexit.

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We offer an unparalleled EU legal representation service for UK sponsors affected by Brexit; with expertise, speed and simplicity.

The leading experts in EU representation and regulatory affairs

With over 25 years’ experience, our experts can manage all of your EU representation and regulatory affairs requirements. You can relax – safe in the knowledge that our experts will ensure your continued compliance post-Brexit.

We make it simple to remain compliant post-Brexit

Our locations in London and Dublin offer us a short cut to registering a change of EU legal representation through the consistency of common law legal systems and of our shared English language. This unique offering means we can very simply ensure your continued compliance post-Brexit.

We make it easy to remain compliant post-Brexit

Our locations in London and Dublin also provide a short cut to registering a change of EU legal representation through the consistency of Common Law legal systems and shared English language. This unique offering means we can ensure your continued compliance post-Brexit quickly and without fuss.

Protect your clinical trial

Will your clinical trial meet legal requirements post-Brexit? Speak to our experts who will advise and support you in ensuring your continued legal compliance post-Brexit.

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The leading experts

Ensuring your product reaches patients without unnecessary delay

Founded in 1994, we are the leading experts in maximising access to the EU market, helping your product reach as many patients as possible. Our expertise spans pharmaceuticals and biotechnology across both EU representation and regulatory affairs services.

Contact Us

Fill out this form and one of our experience experts will contact you directly to help ensure your continued compliance post-Brexit.

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Frequently asked questions

We understand that conflicting advice can make legal and regulatory compliance confusing. That’s why our experts in this field have created these FAQs to help you simply and quickly understand the requirements and how we can support you to ensure your continued compliance post-Brexit:

Why does the sponsor need a legal representative in the EU?

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What advice does the European Commission provide to UK sponsors regarding EU clinical trials once the UK becomes a third party following its withdrawal from the EU (“Brexit”)?

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If the study is in the UK, and the sponsor is outside of the UK/EU, can the sponsor retain the UK legal representative?

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Does the sponsor need a different legal representative for each EU trial?

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How long does it take to initiate legal representation?

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Which countries are covered by IDEA’s legal representation?

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What are the main advantages to the sponsor using IDEA as a legal representative compared to a CRO?

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How much does legal representation cost and what do the costs cover?

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