PCG Clinical Services is a Scandinavian full-service CRO that’s committed to improving clinical trials through our scientific expertise, progressive technology and more effective ways of working. Our capabilities range from early study advice through Phase I to Phase IV trials, supported by our flexible global partner network.
Our Senior Advisory Team offers a wealth of clinical development expertise to guide you through study design, study conduct and regulatory requirements. Through their exceptional combined experience, our advisors will help you find the most effective design to achieve your study objectives and deliver high quality data. Our range of Phase I-IV services includes project management, clinical operations, biometrics, EDC, medical writing, quality assurance, auditing and validation. We deliver clinical studies through the cutting-edge Viedoc™ EDC system, for robust and accurate data handling. It provides highly efficient data capture, powerful query flagging and intelligent data monitoring for all types of trials.
PCG has been in operation since 2003 and has grown to 65+ employees. To date we have delivered 350+ studies in 24 countries, across all therapy areas with a strong focus in phase I/II. Our highly qualified people have been trusted by some of the most advanced drug developers to manage studies across extensive therapeutic areas. Our risk-based monitoring process and comprehensive quality system ensure that we provide you with high quality, regulatory compliant data in which you can have the utmost confidence. With more than 100 audits accomplished to date, you can rely on the PCG team and our values to take your product to the next stage.