Compliance With EU MDR and UK MDD

Navigating multiple regulatory environments is not uncommon for global companies. However, it can be difficult to implement mandated changes close to home, especially when multiple quality regulations are changing at once.

Read this brief to learn the differences between UK and EU regulations for medical device manufacturers. See how an electronic quality management system (eQMS) can help you achieve dual-regulatory compliance and give you an edge against your paper-based competitors who are struggling to catch-up.

  • Differences between UK and EU regulatory bodies and processes.
  • Impacts on medical device manufacturers.
  • How an eQMS reduces the cost and effort of compliance.
  • What actions are needed to get and keep products on the market.
How To Navigate UK and EU Quality Regulations in a Post Brexit World