Regulatory Strategy

Virtually everything a company does during the development phase of a product's life is aimed at satisfying the regulators of its quality, safety and efficacy. RRG's approach recognises the importance of a living, comprehensive regulatory plan to support your product from conception through to the end goal – successful marketing.

At RRG, we have many years of experience in advising companies on effective strategies to get their products to market. We work in partnership with our clients to provide regulatory advice and strategy that covers the full range of development activities from preclinical development right the way through to marketing authorisation and product life cycle management.

This is facilitated by:

  • The extensive experience of all our consultants in global regulatory affairs and product development
  • An expert knowledge of the regulatory requirements across a wide range of therapy areas and product formulations
  • The preparation of detailed strategy documents
  • The anticipation of problems and issues and the development of plans to address them
  • A wide network of contacts
  • A detailed understanding of the regulatory procedures across a range of markets
  • A broad experience of scientific advice meetings at national and EMA level
  • A track record of successful submissions for clinical trial and marketing authorisations

Contact Us

T: +44 (0)1276 671 166
F: +44 (0)1276 670 960

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RRG, Innovation House
Albany Park, Camberley
Surrey. GU16 7PL

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