Clinical Monitoring for your clinical trial

GWT - Your partner for effective clinical monitoring

Welcome to the clinical monitoring division of GWT - Society for Knowledge and Technology Transfer. Our dedicated team of CRAs (Clinical Research Associates) with many years of experience in monitoring research projects and contract research is ready to ensure the monitoring of your clinical trials with various indications. We specialize in hematology, oncology, diabetes, dermatology, pulmonology and cardiology.

Your benefits at a glance

Nationwide network for wide reach in clinical trials and support of trial sites.
Quality and efficiency for successful studies and high data quality.
Experienced CRAs offer comprehensive support throughout the entire study process (conception, study design, processing, review, quality control).
Close cooperation for the highest quality standards and patient safety.
Clinical monitoring for fast, effective time-to-market of your products.

Photo; female doctor with stethoscope and patient file, she writes with a pencil

Clinical Monitoring - Quality, experience, collaboration: Our services for advancing your clinical excellence.

⌈ Implementation of various monitoring visits
⌈ Site selection visits, initiation visits, regular on-site monitoring
⌈ Remote monitoring, close out visits
⌈ Preparation of study documents (monitoring plan, report templates)
⌈ Query management and data cleaning support
⌈ Site management as primary contact person for the centers
⌈ Conducting and reporting on monitoring visits
⌈ Implementation of the drug account
⌈ Document management and review of study folders

GWT - Your expert for successful Clinical Monitoring!

⌈ Superior Quality: Quality and efficiency of clinical monitoring ensure high data quality studies
⌈ Experienced Support: Experienced CRAs provide comprehensive study lifecycle support
⌈ Collaborative Excellence: Close collaboration with study sites and PIs enhances quality standards and patient safety

Photo; team of doctors and the monitor sit at a table and look through patient files.

Effective clinical monitoring with GWT experts

Dr. Linda Hein

Clinical Monitoring Specialist

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Phone:
+49 351 25933 179

Email:
linda.hein@g-wt.de

Nathalie Pfeiffer

Clinical Monitoring Specialist

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Phone:
+49 351 25933 167

Email:
nathalie.pfeiffer@g-wt.de

GWT: ICH-GCP compliant monitoring - safety, quality control & success guaranteed for your clinical trials!

GWT - your partner for ICH-GCP-compliant clinical trial monitoring: We guarantee the protection of study participant rights, correctness and completeness of the collected data as well as compliance with study plans and legal requirements. Our experienced CRAs support you before and during the study and contribute significantly to the success of your clinical trials. Benefit from our expertise and nationwide network in the fields of hematology, oncology, diabetes, dermatology, pneumology and cardiology.

Sponsor oversight for clinical trials

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.

Clinical Quality Management

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.

Clinical Safety

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.

Clinical Study Promotion

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.

Thank you for your interest in our services. We gladly answer your enquiries!

Location Dresden

+49 351 25933 100

Location Berlin