Specific Services for UK and Ireland

The Medicines and Healthcare products Regulatory Agency (MHRA) is responsible for regulating all medicines and medical devices in the UK by ensuring they work and are acceptably safe.

Our UK based consultants can provide support and advice for all your project requirements. Specific services provided by our team in the UK include:

• Advice and interpretation of UK and Ireland regulations
• Interaction and meetings with the UK and Irish Authorities (MHRA and HPRA respectively)
• Regulatory support for clinical trials
• Compliance with the ABPI code of practice