Adriaus Consulting is a niche and boutique consultancy dedicated exclusively to the biopharmaceutical, biotechnology and pharmaceutical medicine industries. We offer the full range of expertise and services in Global Regulatory Affairs, Regulatory Strategy and Project Management for vaccines, biological, biotechnology and pharmaceutical medicines. Our expertise and interests stretch across all stages of product development, commercialisation and life-cycle management.

If your goal is to take your development program and product globally, our experience and expertise will facilitate your success. If your goal is to focus your development program, commercialisation and life-cycle management regionally, we can lead and support you to get the required result.

We have a proven track record of success in Global Regulatory Affairs with the United States’ Food and Drug Administration (FDA), the Therapeutic Goods Administration (TGA), the European Medicines Agency (EMA), Medsafe and others. Our ongoing success in Global Regulatory Affairs is underpinned by outstanding competencies and skills in Regulatory Strategy and Project Management. We pride ourselves on achievement and realisation of business objectives, through high quality and timely delivery of regulatory solutions, submissions and approvals. We leverage our extensive, broad and in-depth experience for advancement and success of our client’s projects. We continuously educate and develop ourselves to keep abreast of emerging regulatory and environmental issues and assess how they may impact on our client’s development programs, projects and products.