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Discover an informative webinar to unravel the complexity of the Clinical Trials Information System (CTIS) and explore the regulatory structure in Europe. Most importantly, let’s discuss whether all the latest changes in the regulatory landscape still position Europe as the number one destination for clinical trials.
GCP-Service is a trusted CRO partner specializing in accelerating global clinical trials with reliable solutions for medical innovations. With full-service management solutions for all classes of medical devices and pharmaceutical trials, GCP-Service ensures excellence in clinical research. Our experienced team and diverse clinical study expertise enable us to provide tailored services, including clinical operations, biostatistics, trial master file and document management, clinical data management, regulatory affairs, project management, product vigilance services, legal representation, medical and scientific writing, and sponsorship as a service. We also offer GCP training through a range of online and face-to-face courses and events.