Sponsor oversight for your clinical trial

Die GWT — your partner as an independent clinical sponsor for comprehensive clinical trials

GWT - Society for Knowledge and Technology Transfer is your reliable partner in the field of Sponsor Oversight and independent, clinical sponsor for Investigator Initiated Trials (IIT studies), Medicines Act (AMG) studies, Medical Devices Act (MPG) studies and Non-Interventional Studies (NIS) studies. As a service provider, we are responsible for your clinical trials and research projects.

Your benefits at a glance

Over 25 years of experience in international, multi-site clinical trials of diverse medical indications.
Extensive expertise and quality in hematology, oncology, immunotherapy, pneumology and more.
Efficient, cost-effective access to patient populations through European trial site network.
Expert teams in project management, safety/PV, data management, monitoring, regulatory affairs and administration.
Smooth, professional implementation of your clinical trials through expert support.

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GWT - your innovation through expertise and network in clinical research

Working with GWT means that you will benefit from our many years of experience and our extensive network. We always strive to meet your requirements in the best possible way and to develop innovative solutions that meet current and future clinical research requirements.

GWT - Your trusted partner for groundbreaking success in clinical research

Trust GWT as your partner for sponsor oversight and independent sponsor in clinical research. Together, we will set new standards and work hand-in-hand for the success of your clinical trials.

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Sponsor oversight with GWT experts

Petra Gerteis

Clinical Safety Specialist

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Phone:
+49 351 25933 124

Email:
petra.gerteis@g-wt.de

Franziska Hoppe

Teamleitung Clinical Monitoring

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Phone:
+49 351 25933 180

Email:
franziska.hoppe@g-wt.de

Dr. Carsta Köhler

Fachliche Leitung Bereich Medizin

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Phone:
+49 351 25933 190

Email:
carsta.koehler@g-wt.de

Wera Kupetz

Teamleitung Clinical Safety

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Phone:
+49 351 25933 173

Email:
wera.kupetz@g-wt.de

Susann Leupold

Business Development Account Managerin

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Phone:
+49 351 25933 197

Email:
susann.leupold@g-wt.de

Nathalie Pfeiffer

Clinical Monitoring Specialist

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Phone:
+49 351 25933 167

Email:
nathalie.pfeiffer@g-wt.de

Jana Plätschke

Senior Clinical Regulatory Specialist

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Phone:
+49 351 25933 126

Email:
jana.plaetschke@g-wt.de

Dr. Anna Polowinski

Klinischer Projektmanagerin

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Phone:
+49 351 25933 171

Email:
anna.polowinski@g-wt.de

Martin Puttrich

Teamleitung Clinical Quality Management und Prozessdigitalisierung

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Phone:
+49 351 25933 193

Email:
martin.puttrich@g-wt.de

Corina Röllig

Klinische Datenmanagerin

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Phone:
+49 351 25933 174

Email:
corina.roellig@g-wt.de

Dr. Michael Unger

Teamleitung Clinical Data Management

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Phone:
+49 351 25933 181

Email:
michael.unger@g-wt.de

Dr. Carmen Weigt

Senior Klinische Projektmanagerin

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Phone:
+49 351 25933 172

Email:
carmen.weigt@g-wt.de

GWT: Your independent clinical sponsor partner for research excellence and customized solutions

GWT - Your experts for ICH-GCP compliant sponsor tasks: Comprehensive expertise and prudent strategies to ensure patient safety, data integrity and efficient risk management in clinical trials. Rely on over 25 years of experience and our dedicated teams.

Clinical Monitoring

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.

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 Design Advice

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.

Preclinical Study Advice

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.

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

Dr. Carsta Köhler

Fachliche Leitung Bereich Medizin

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Phone:
+49 351 25933 190

Email:
carsta.koehler@g-wt.de

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Expiry:	30 Tage
Location:	Localstorage
Description:	Saves the storage period of the privacy level settings from the cookie consent tool "Privacy Manager".