Legal representation is essential for conducting EU clinical studies, ensuring compliance, smooth execution, and serving as a key regulatory bridge.
Both models enhance your clinical trial. Our flexibility allows us to provide our expertise where needed and we can work according to clients SOPs or with our own SOPs.
Both models enhance your clinical trial. Our flexibility allows us to provide our expertise where needed and we can work according to clients SOPs or with our own SOPs.
Our biostatistics team optimizes clinical trial design, creates statistically sound, compliant protocols, and maximizes the insights you gain from your trial analysis.
At GCP-Service we believe that TMF oversight, control, and inspection readiness are vital to the success of your clinical trial.
The safety of patients always comes first, and we help you seamlessly navigate recording, processing and reporting requirements of all safety-related events!
The regulatory start-up process is critical for clinical trials. Delays can impact study timelines. We ensure a timely start-up for your trials!
We support clients developing innovative products, including pharmaceuticals and medical devices, across all clinical development stages.
Our PM team at GCP-Service ensures expert study coordination, delivering oversight, transparency, and seamless execution across all phases.
Data matters! In clinical trials, success depends on strong data governance, infrastructure, and ecosystem to ensure quality, integrity, and insights.
Whether it’s a publication, study protocol, or report – delivering a clear, accurate message is always at the heart of it.