DRACO Consulting is a newly created Regulatory Affairs services company with a specific business idea: providing high level and customized technical and regulatory services to HealthCare companies. Composed of a team of professionals with decades of experience in pharmaceutical multinational companies, DRACO operates in Europe and Asia (China). Flexibility, reactivity and customer customization are our main focus to offer a tailor-made support to our customers. Large scale or smaller scale projects ? Total or partial outsourcing ? DRACO is willing to consider the most suitable solution for your organization. Among its global expertise within Regulatory Affairs, DRACO proposes specific services for non EU based companies wishing to develop their business in Europe, such as EDQM certification, Drug Master File writing, WHO pre-qualification of medicines.