BlueReg sees your projects through to success


BlueReg offers customised and individually adapted solutions, which will consider trends and factors that will have a future impact on the market access of your products regardless of the size or timeline of the project.
Our team is available when you need them – where you need them:

  • small to large outsourcing projects
  • customer on-site support
  • ad-hoc regulatory advice
  • maternity leave/paternity leave/sickness absence

Support can be provided within any of our offices.

A team of experienced consultants

The pharmaceutical industry is governed worldwide by a set of highly complex and evolving regulatory frameworks. Navigating and executing the best pathway requires expertise and resources not always available within companies.

BlueReg proposes a flexible approach and a dynamic team with extensive hands-on industry experience for your projects in drug development, regulatory affairs, quality management and pharmacovigilance.

Our team includes drug development, regulatory affairs, quality and pharmacovigilance specialists including those with PhDs, Pharm.D.s/MPharms and MDs who have significant expertise and practical experience acquired within the pharmaceutical industry

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