Canary Regulatory Affairs is a consultancy established to help bring new treatments to patients globally. Canary can assist at all stages of product development, from the selection and project management of suppliers for raw materials and specialised GMP, GLP and GCP compliant service providers, to the preparation of study protocols and reports. Our expertise covers Quality, Non-Clinical and Clinical. We support product registration by establishing an early dialogue with international Regulatory Authorities and through the preparation of regulatory dossiers. Canary can help you navigate any regulatory hurdle in Australia, the European Union, the United States and beyond, leading to resolution through negotiation of any issue encountered. We will work cooperatively with all stakeholders, as we believe that constructive relationships create goodwill and are paramount to problem solving. We love to learn and stay informed on new developments and legislative requirements, take up new challenges and find the right answers. We pride ourselves on high quality and timely delivery and will take care of your projects as if they were our own.