Study Center

Our study team has years of experience with running multicentric clinical trials. We have conducted over 200 studies in phase II – IV, including AMG (national drug law), MPG (medical device law), and pilot studies.

Our expert team consists of medical doctors, study nurses, study coordinators, recruitment staff, and external medical consultants who guarantee best practice in conducting your trial.

We work in close collaboration with the Charité (Europe’s largest university hospital) in Berlin as well as with other polyclinics. Thus, we can offer a broad spectrum of analytical methods such as state of the art diagnostics along with bedded unit capacities (incl. sleep lab).

Our strict SOP–based quality management system is in line with ICH-GCP requirements, national drug law (AMG), and medical device law (MPG). We constantly train our staff in GCP, SOPs and regulatory affairs. Additionally, we have undergone numerous internal and external audits.

Expertise and Competencies

It is key for us to use multiple recruitment strategies to lead your trial to success by reducing timelines and costs. In addition to using targeted advertisement types such as e.g. public transport, daily newspapers, study-specific print and digital media, direct contact etc., we have our own comprehensive subject database at our disposal.

Our core competence lies in the fields of phytopharmaceuticals, Rx/OTC, food products (food supplements, functional food, PARNUT/FSMP), medical devices, and cosmeceuticals.

We provide an extensive network of analytical and diagnostic laboratories as well as temperature- and humidity-controlled storage capacities for IP, archiving rooms, and several examination rooms for subject visits.