In a fast-moving and continuously expanding pharmaceutical industry, the need for efficient and well-documented clinical trials is evident. A Clinical Research Organisation (CRO) is a service organisation dedicated to the pharmaceutical and biotechnology industries, offering value-added services to promote the research and development process. The Nordic CRO IRW manages clinical trials from start to finish, or function as a fully-integrated part of a client’s study team depending on the clients’ need.
IRW is a full-service CRO founded in 1999 by Ingela R. Wiking. IRW has local offices in Sweden, Norway, Finland and Denmark and offers a broad spectrum of comprehensive services to companies and institutions operating over both geographical and scientific boarders.
Managing projects from start to finish
The IRW team is dedicated and professional representing a wide range of academic competence, possessing solid experience of Clinical Research, Pharmacovigilance, Data Management, Biostatistics and Medical Writing. “A substantial part of our team comes from global pharmaceutical and biotech companies”, Ingela Wiking, CEO, explains.
“We also have great insight and experience of working with the regulatory authorities in the Nordic countries. This, in combination with our well-established competence of clinical research, enables us to manage projects from start to finish, or function as a fully-integrated part of our client’s team”.Tailored Services
IRW offers management of phase I-IV pharmaceutical trials, covering projects ranging from single centre to multinational large-scale trials. IRW has the resources and knowledge necessary to continuously monitor the safety of pharmaceutical drugs through clinical development and post-authorisation. As a full-service CRO, IRW also offers Data Management and Biostatistics.
“We offer services tailored to the needs of our clients. We can deliver a complete solution –, or standalone services covering a certain aspect of our client’s business”.
Able to secure management
More than ten year’s experience in the field of clinical trials has enabled IRW to build up an extensive network – from Scandinavia and Europe to the USA.
“Our clients range from small start-up companies to multinational pharmaceutical corporations. We are able to meet our clients’ high demands and maintain projects efficiently, bridge a temporary shortage of experienced staff and secure temporary management, if needed”, Ingela Wiking concludes.