Our services for your clinical trial

GWT is your reliable partner for independent clinical sponsorship. Over 25 years of experience in IIT, AMG, MPG studies and NIS with expertise in hematology, oncology, immunotherapy, pneumology, metabolism, angiology and cardiology. Our European network ensures efficient patient access. Our expert teams in project management, safety/PV, data management, monitoring, regulatory affairs and administration provide clinical research excellence and tailored solutions.

Our team of experts and European trial site network ensure structured planning, efficient communication and reliable monitoring. Rely on us for smooth study execution and optimal patient care.

Our team of experts and European network ensures excellent administration, structured organization & continuous communication. Successful research goals & improved patient care with GWT as a reliable partner.

Our expertise in organization, eCRF design, data preparation & validation for IIT & AMG studies ensures data quality & integrity in multicenter, multinational projects - for optimal therapies & better patient care.

Trust our team of experts for safety and data integrity in IIT, AMG and MPG studies. We provide GCP-compliant QM documents, audits and inspection support for highest study quality.

Our expertise in IITs, NIS and PASS studies ensures seamless recording and reporting of SAEs, and early risk identification and transparent communication. Our experienced team and network ensures patient safety and data integrity according to ICH-GCP guidelines - for successful studies.

Our experienced CRA team and nationwide network ensures comprehensive support in hematology, oncology, diabetes, dermatology, pulmonology and cardiology. We guarantee ICH-GCP-compliant monitoring, patient safety, high data quality and compliance with test plans and laws.

GWT offers a holistic approach to increase the visibility of your studies, effectively identify and recruit study sites and participants. To this end, GWT offers evaluation of suitable study sites, implementation of effective patient recruitment strategies, and provision of a multinational personal contact for smooth operations and optimal results in clinical trials.

GWT supports you in experiment design, statistical analysis, pharmacology, toxicology, GMP manufacturing, analytics, scientific advice (PEI, BfArM) and scientific writing. Benefit from our expertise in preclinical advice, regulatory requirements (EMA, FDA). We support you in experiment design, statistical analysis, pharmacology, toxicology, GMP manufacturing, analytics, scientific advice (PEI, BfArM) and scientific writing.

Support for clinical trials (Phase I-IV), non-interventional studies, scientifically initiated studies, Medical Device Act studies and market approval studies. GWT offers long-standing expertise in patient and study site planning for multicenter/multinational projects with a specialization in hematology, oncology, pulmonology, dermatology and ophthalmology.

Targeted insights for indications such as pulmonary disease, diabetes, cardiovascular disease, and hematologic disease improve clinical trials through real patient data, in-depth analysis of big data, and better understanding of therapeutic approaches.