European-trained MDs providing consulting services to pharma, device manufacturers, academia and biotech. Wide-ranging medical affairs and clinical development expertise, in oncology, infectious diseases, hepatology, anemia and more. We work with clients in North America, Europe, Asia and Australasia, either remotely or in person. Our regulatory department provides both strategic and operational expertise across a broad spectrum of the industry, including pharma, biologics, devices, quality systems, compliance and eCTD services. Our e-publishing services include authoring, e-publishing, compilation, validation and submission of eCTDs in US and ROW.