Specific Services for UK and Ireland

Our market 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


  • ABPI signatory (copy approval) for promotional materials
  • Providing advice to your marketing team on product claims
  • Wholesaler dealers licence applications (WDL) / Manufacturer/importer licence (MIA)
  • Advice on setting up supply chains and distribution requirements
  • Attendance at MHRA and HPRA scientific advice meetings
  • Pharmacovigilance support