We cover the full range of projects from single-center to multi-national, offering professional Clinical Trial Management, Regulatory Submission, Medical Writing, Data Management, Biostatistics, Pharmacovigilance and Quality Assurance services for pharmaceutical, biotechnology and medical device companies. We can manage your project from start to finish, or function as a fully-integrated part of your study team.
In all Nordic countries, we have experienced native-speaking experts handling all regulatory and ethical submissions, as well as local monitoring services and support-to-site. This, together with an excellent network of local investigators, will speed up the regulatory processes, as well as facilitating communication with sites and investigators.
We conduct all our work according to applicable current regulations and guidelines, Sponsor or IRW SOPs. All our procedures and data collected are subject to our in-house Quality Assurance. Being a local Nordic CRO, we can provide you with our wide-ranging knowledge on local networks, including investigators, both within the private and academic institutions.