IRW are experts in interacting with Nordic regulatory authorities. We cover the full range of CRO services throughout your products' lifecycle, for studies of all sizes and through all phases and beyond, acting either as a full-responsibility partner or provider of in-sourced expertise.

The IRW team is dedicated and professional, with a wide range of academic competence and solid experience of clinical research, as well as of working with global pharmaceutical and biotech companies, and of interacting with the various regulatory authorities in the Nordic region.

Clinical trial management, data management, biostatistics and pharmacovigilance services

We cover the full range from single-centre to multi-national projects, offering professional clinical trial management, data management, biostatistics and pharmacovigilance 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.

At IRW, we are aware of the fact that our customers need to cut timelines and be cost-effective when bringing an investigational product up to registration. 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 communications with sites and investigators.

We conduct all our work according to current regulations and guidelines i.e. ICH-GCP, local ethical requirements, the Helsinki Declaration and 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 sector and in state-run institutions.