Experts of GCP-Service International
Our excellence is your success. The expertise of the GCP-Service team in different types of clinical studies is one of our key values we provide to our clients. Our focus on agile small to midsize clients requires a special mindset of our experts which we develop and improve since the foundation of GCP-Service. The involvement of our experts ensures that the conduct of a huge variation of clinical studies, with its different study designs, objectives, products, medical areas in several geographical regions reach the goal. The fact that our experts work hand in hand to smooth the entire development process is unique in the CRO world. We are proud to introduce our pleasant expert team responsible for the cost-effective conduct of your studies as professionals and as humans:
Board of Directors
Process/System experts
Medical Device Consultancy Task Force Group
The goal of this Group is to help medical device manufactures with preparation to both the new Medical Device Regulation (MDR) and the new In Vitro Diagnostic Regulation (IVDR). We want to help companies to bring light into the dark. The Task Force Group works closely with our International Advisory Board that assures medical expertise truly throughout all therapeutic areas. Our multifunctional team can support you with:
– Development of a study design that proves the performance and safety of your product
– The sample size calculation to collect robust data
– Preparing an investigational plan
– Train your staff in the conduct of clinical trials with medical devices
– The selection of reliable investigators and cost-effective countries
– Preparing Clinical Evaluations
– Regulatory consultancy
– All other tasks which might help you to bring your product to the market.
