Clinical Monitoring

Nationwide network for wide reach in clinical trials and support of trial sites

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

Franziska Hoppe

Team Leader Clinical Monitoring

Nathalie Pfeiffer

Clinical Monitoring Specialist

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.

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Sponsor Oversight
GWT: Your independent sponsor for comprehensive clinical trials

Clinical Project Management
Comprehensive coordination of all aspects of your clinical trial

Clinical Project Administration
Seamless communication and administration of your clinical trial

Clinical Data Management
Ensuring the highest quality and 100% integrity of your clinical data

Clinical Quality Management
Highest quality standards in the supervision of your clinical trial

GWT StudyDesigner

Transform your study design with GWT StudyDesigner - Real-time interactive design and expert advice for your clinical research!

Project Administration
Efficient administrative implementation of industrial projects

Contract Management
Individual consulting for legally compliant transfer projects

Financial Management
Ensuring and carrying out correct financial transactions

Startup Backoffice

Turn your ideas into action - supported by GWT's comprehensive business platform.

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