Established in 1990, RRG has many years of practical US/EU regulatory experience. RRG provide pharma/biotech clients with global regulatory strategy, product development and regulatory submission support plus comprehensive, bespoke regulatory training programmes. 75% of work is repeat business, over 90% comes from referrals.

RRG has continued to develop its services and expertise since it was established in 1990. RRG have a team of highly experienced regulatory consultants who all have at least 10 years experience and have previously held senior posts in industry, consultancy or regulatory authorities.

RRG offers an extensive range of regulatory services and expertise to the pharmaceutical industry, helping companies to manage every stage of the drug development process. RRG also support other companies working in the healthcare field, for example medical device suppliers.

Services include: Product Development, Regulatory Strategy, Regulatory Submissions, Training and User Testing.