Our team is experienced in providing service in all phases of clinical development for pharmaceutical, medical device and functional food trials. We provide a full-service concept offering the entire study team for all functions, or professionals working as a part of the customers’ study team.

A new level of customer attention, flexibility and reliability is brought to you by Crown CRO from early regulatory consulting all the way to medical device trials and CE-mark and 510(k) submissions.

Crown CRO Quality Assurance Services can support you to develop, implement and update your quality systems and procedures to conform to current guidelines and regulations. We also provide auditing services to help you identify your strengths, as well as areas that need improvement.

Meeting clinical study or post-marketing pharmacovigilance (PV) obligations is a key requirement for your company. If you need resources or know-how, the Crown CRO PV team can offer personalized services either to strengthen your own PV functions or as a full-service PV solution.

Do you need high quality translations for your clinical trials, drug regulatory affairs or pharmaceutical marketing? Crown CRO Medical Translations can offer you all of those and much more. Go to our Medical Translations page for more information and contact details.

Our Regulatory Affairs function supports your goals by providing a broad variety of flexible and cost-effective Regulatory Affairs services. Our main services cover clinical trial application submissions, regulatory strategies and documentation as well as regulatory procedures for pharmaceuticals and medical devices.

Crown CRO supports pharma and biotech companies and other CROs with study rescue operations. A fresh point of view, new ideas or simple support and motivation can help to put the study back on track and bring it to a successful conclusion.