Real Regulatory offers clients access to a team of proven experts in regulatory affairs. The service includes consultancy and hands-on assistance to pharmaceutical and medical device companies. The company positions itself as a provider of regulatory services for clients wishing to gain strategic advice and practical assistance in obtaining approvals to market these products in the EU.

The Real Regulatory team consists of dedicated and experienced graduate level professionals with extensive experience gained by working in a variety of organisations, ranging from large ethical multinationals through to small and medium sized companies, specialising in new chemical entities and generic type products.

Our extended team extends throughout Europe and beyond, and comprises a network of independent in-country consultants, who give country specific advice, covering all EU and non-EU European countries. We also offer regulatory expertise in many specialised areas and resources can be brought in and expanded for clients as needed for any given contract. This additional resource can be scaled back down again immediately when not required.

Our expert contributors provide support and advice on a wide range of topics including:

  • Regulatory
  • Clinical
  • Pharmacology
  • Toxicology
  • Quality
  • Statistics
  • GxP and supply chain issues
  • Pharmacovigilance

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