Regulatory Resources Group   Established in 1990, the company provides a range of regulatory services to the pharmaceutical industry, helping companies to manage every stage of the drug development process. This may include the design of the regulatory and clinical strategy through to the preparation and management of the dossier during the regulatory approval process. After the product has been marketed, we frequently plays a role in the subsequent management of the product life cycle. Training is a large and growing part of our service and we provide external courses and a range of in-house programmes that are tailored to meet the client’s requirements. Our services are designed to meet the needs of every type of organisation, large or small. We can support the in-house Regulatory Affairs Department by undertaking specific projects and by providing ongoing staff training. Alternatively, we can take overall responsibility for a project and manage the entire regulatory process.