Regulatory Services 

RenaClinical’s regulatory team can provide advice on navigating the complex EU legislative framework for clinical trial applications. 

  • QP Supply Chain Assessments

  • CTA application support & drafting

  • Providing strategic advice on MHRA, EU, and US regulatory processes

  • Authoring IMPDs and simplified IMPDs

  • Support and presenting at MHRA and EMA scientific advice meetings

  • Commercialisation planning at early phase clinical development